Invacare Corporation

8 devices in the database

  • Model / Serial
    The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098, 10JF034099, 10JF034100, 10JF034101, 10JF034102, 10JF034103, 10JF034104, 10JF034105, 10JF034106, 10JF034107, 10JF034108, 10JF034109, 10JF034111, 10JF034112, 10JF034113, 10JF034114, 10JF034115, 10JF034116, 10JF034117, 10JF034119, 10JF034120, 10JF034121, 10JF034122, 10JF034123, 10JF034124, 10JF034125, 10JF034126, 10JF034127, 10JF034128, 10JF034129, 10JF034130, 10JF034131, 10JF034132, 10JF034133, 10JF034134, 10JF034135, 10JF034136, 10JF034177, 10JF034178, 10JF034179, 10JF034180, 10JF034181, 10JF034182, 10JF034183, & 10JF034184.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide distribution: USA including states of: FL, GA, KY, LA, MO, NC, NE, NJ and SC.
  • Product Description
    HomeFill Oxygen Compressor IOH200 Homefill, The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098, 10JF034099, 10JF034100, 10JF034101, 10JF034102, 10JF034103, 10JF034104, 10JF034105, 10JF034106, 10JF034107, 10JF034108, 10JF034109, 10JF034111, 10JF034112, 10JF034113, 10JF034114, 10JF034115, 10JF034116, 10JF034117, 10JF034119, 10JF034120, 10JF034121, 10JF034122, 10JF034123, 10JF034124, 10JF034125, 10JF034126, 10JF034127, 10JF034128, 10JF034129, 10JF034130, 10JF034131, 10JF034132, 10JF034133, 10JF034134, 10JF034135, 10JF034136, 10JF034177, 10JF034178, 10JF034179, 10JF034180, 10JF034181, 10JF034182, 10JF034183, & 10JF034184. || The IOH 200 Homefill is an electromechanical, prescription device designed for use in the home. Its intended function and use is to provide supplemental oxygen to patients and to supply pressurized oxygen to fill cylinders for the patients personal ambulatory use.
  • Model / Serial
    Model Numbers: 0806281234, 0806893858, 0806135534, 0806161578, 0806237627, 0806268153, 0806268154, 0806309590, 0806315524, 0806351557, 0806568768, 0806591793. 0806670117, 0806724855, 0806731287, 0806773921, 0807007811, 0807019897, 0807062866, 0807110193
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Product was distributed to the following states: CA, CO, MN, NJ, OR, PA, TX & VA and one to Canada.
  • Product Description
    Kuschall K Junior Manual wheelchair
  • Model / Serial
    06JE002273, 06JE002762, 06JE003580, 06JE003583, 06JE003584, 06JE003585, 06JE003597, 06JE003598, 06JE003880, 06JE003890, 06JE004170, 06JE004172, 06JE004178, 06JE004196, 06JE004632, 06JE004640, 06JE005420, 06JE005421, 06JE005864, 06JE005870, 06JE005871, 06JE005879, 06JE005885, 06JE006254, 06JE006277, 06JE006599, 06JE006603, 06JE006612, 06JE007087, 06JE007393, 06JE007396, 06JE007403, 06JE007408, 06JE007818, 06JE008028, 06JE008311, 06JE008322, 06JE008324, 06JE008329, 06JE008330, 06JE008332, 06JE008350, 06JE008670, 06JE008678, 06JE009028, 06JE009031, 06JE009039, 06JE009040, 06JE009042, 06JE009060, 06JE009062, 06JE009076,  06KE000147, 06KE000149, 06KE001924, 06KE001933, 06KE002243, 06KE002264, 06KE002265, 06KE002267, 06KE002270, 06KE002851, 06KE002853, 06KE002858, 06KE002862, 06KE003116, 06KE003379, 06KE003381, 06KE003386, 06KE003612, 06KE004451, 06KE004454, 06KE004455, 06KE004467, 06KE004854, 06KE005538, 06KE005826, 06KE006063, 06KE006065, 06KE006333, 06KE006613, 06KE006876, 06KE006877, 06KE006886, 06KE006894, 06KE007257, 06KE007282, 06KE007294, 06KE007450, 06KE007684, 06KE007686, 06KE007689, 06KE008610, 06KE008611, 06LE000170, 06LE000173 06LE001305, 06LE001313, 06LE001527, 06LE001694, 06LE001696, 06LE001697, 06LE001705, 06LE001998, 06LE002608, 06LE003258, 06LE003261, 06LE003267, 06LE003268, 06LE003462, 06LE003466, 06LE003987, 06LE004643, 06LE004650, 06LE004846, 06LE004857, 06LE005143, 06LE005144, 06LE005148, 06LE005152, 06LE005154, 06LE005732, 06LE005895, 06LE006012, 06LE006013, 06LE006024, 06LE006704, 06LE006707, 06LE006709, 06LE007018, 06LE007210, 06LE007358, 06LE007371, 06LE007379, 06LE007387, 06LE007393, 06LE007397, 06LE007403, 06LE007404, 07AE000983, 07AE001149, 07AE001180, 07AE001326, 07AE001327, 07AE001334, 07AE001594, 07AE001595, 07AE002009, 07AE002013, 07AE002223, 07AE002225, 07AE002229, 07AE002400, 07AE002404, 07AE002670, 07AE002683, 07AE002990, 07AE003522, 07AE003700, 07AE003712, 07AE003713, 07AE003716, 07AE004618, 07AE005103, 07AE005337, 07AE005339, 07AE005340, 07AE005341, 07AE005586, 07AE005593, 07AE005597, 07AE005886, 07AE005887, 07AE005895, 07AE006089, 07AE006303, 07AE006308, 07AE006314, 07AE006927, 07AE006930, 07AE007089, 07AE007090, 07AE007091, 07AE007092, 07AE007103, 07AE007105, 07AE007113, 07AE007114, 07AE007326, 07AE007327, 07AE007331, 07AE007334, 07AE007598, 07AE007606, 07AE007607, 07AE007611, 07AE007612, 07BE001073, 07BE001076, 07BE001077, 07BE001078, 07BE001082, 07BE001093, 07BE001303, 07BE001309, 07BE001310, 07BE001578, 07BE001585, 07BE001806, 07BE001810, 07BE002005, 07BE002014, 07BE002015, 07BE002253, 07BE002254, 07BE003336, 07BE003337, 07BE003569, 07BE003574, 07BE003582, 07BE003584, 7BE003585, 07BE004719, 07BE004907, 07BE004913, 07BE004916, 07BE006332.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and Canada.
  • Product Description
    Invacare Storm TDX Power Wheelchair, Models: #TDX3-PS, TDX3-SE-PS, TDX4-PS.
  • Model / Serial
    0805007204, 0805040231,0805087799, 0805191275, 0805238718, 0805528869, 0805590456, 0805007205, 0805040233, 0805094654, 0805202392, 0805260264, 0805528870, 0805590458, 0805007206, 0805046010, 0805112919, 0805202409, 0805260267, 0805528879, 0805598707, 0805007207, 0805052515, 0805112920, 0805202410, 0805265355, 0805538825, 0805606638, 0805031769, 0805052531, 0805112921, 0805208212, 0805265356, 0805547691, 0805606639, 0805032072, 0805052780, 0805142288, 0805214576, 0805488915, 0805556308, 0805606650, 0805032078, 0805059713, 0805148474, 0805220731, 0805528850, 0805556313, 0805626956, 0805032082, 0805059770, 0805171786, 0805220813, 0805528852, 0805573454, 0805636805 0805032091, 0805081690, 0805171787, 0805226782, 0805528854, 0805573455, 0805636810, 0805040230, 0805087792, 0805178698, 0805226965, 0805528856, 0805590391, 0805643631, 0805643632, 0805743810, 0805793490, 0805837237, 0805871475, 0805937131, 0806309254, 0805664651, 0805743813, 0805802652, 0805845927, 0805894716, 0805969761, 0806309260 0805671759, 0805771388, 0805802878, 0805845935, 0805894890, 0805977531, 0806309261, 0805685506, 0805776512, 0805807275, 0805850343, 0805894892, 0806273105, 0806309267, 0805702791, 0805776514, 0805807278, 0805855553, 0805900539, 0806281922, 0806315127, 0805710093, 0805780848, 0805807281, 0805860047, 0805900540, 0806281924, 0806315184 0805710275, 0805784712, 0805811158, 0805865040, 0805906053, 0806303957, 0806320300, 0805716215, 0805784713, 0805815571, 0805865041, 0805922688, 0806303963, 0806326394, 0805721816, 0805784714, 0805815575, 0805871470, 0805929066, 0806303965, 0806326395, 0805738220, 0805789076, 0805815809, 0805871471, 0805937122, 0806309167, 0806338838,  0806338840, 0806372582, 0806390080, 0806415186, 0806448589, 0805771388, 0806338842, 0806372583, 0806390081, 0806415385, 0806448735, 0806350846, 0806372585, 0806390082, 0806422077, 0806455546  0806350855, 0806372614, 0806390083, 0806428328, 0806463285, 0806355566, 0806372615, 0806396466, 0806428330, 0806463289, 0806366353, 0806372616, 0806408921, 0806428344, 0806463290, 0806366354, 0806372618, 0806408928, 0806428346, 0806480052,  0806366356, 0806372620, 0806408929, 0806428563, 0806480055, 0806366544, 0806390074, 0806408930, 0806435361, 0806480070, 0806372581, 0806390075, 0806408938, 0806441968, 0806488512.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide and Canada.
  • Product Description
    Kuschall''s K3/K4 Series of Manual Wheelchair, Model Airlite.
  • Model / Serial
    06FE009232
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide and Canada.
  • Product Description
    Solara Spree XT (SPRXT) manual wheelchair.
3 more

15 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Invacare Corporation, 1 Invacare Way, Elyria OH 44035-4190
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Invacare Corporation, 1200 Taylor St, Elyria OH 44035-6248
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Invacare Corporation, One Invacare Way, Elyria OH 44036
  • Source
    USFDA
  • Manufacturer Address
    Invacare Corporation, 1 Invacare Way, Elyria OH 44035
  • Source
    USFDA
10 more