International Medical Devices Database

Manufacturer Address
Interpore Cross International Inc, 181 Technology Dr, Irvine CA 92618-2402
Source
USFDA
4 Events

4 devices in the database

Allogenix;

Model / Serial
Serial Numbers: 079180 & 234760
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide
Product Description
Allogenix; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: 02-3110, Interpore Cross International, a Biomet company (Allogenix DBM products contain human tissue (allograft bone) and are intended for transplantation)

InterGro PLUS

Model / Serial
Serial Numbers: 600107, 600015, 279540, 6000098, 255137, 600550, 600232, 600199, 600180, 279579, 600125, 600126, 600201, 600339, 217530, 783490, 600365, 728840, 608430, 608440, 219980, 882050, 203995, 079160, 788840, 687010, 135970, 247877, 600113, 827220 & 247906
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide
Product Description
InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005, DBM010, DBMW05 & DBMW10, Interpore Cross International, a Biomet company (lnterGro DBM products contain human tissue (allograft bone) and are intended for transplantation)

Device Recall Nexus or Geo

Model / Serial
NEXUS Product List Of Catalog Numbers & Lot Numbers Catalog Number Lot Number/s 1000-3000 300510 303512A 302909A 303012 302812A 302912 302109 303009 1000-3001 326408A 304009 304509 1000-3003 301210 305809A 305509 304709A 305109 324508 1000-3004 304011A 310110 303911A 1000-3005 304211A 312410 301112 304311 1000-3010 302407 300404 1000-3011 313207 1000-3013 307404 312107 312307A 1000-3015 306911A 309505 305605 305905 307111
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
TN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.
Product Description
Spinal Implant, || Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)

Device Recall Interpore Cross International

Model / Serial
Lot #25947 Catalog # 1100-9019 & #1100-9020
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
U.S., Netherlands, Australia, Venezuela, Mexico, Columbia and Brazil
Product Description
C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm

One manufacturer with a similar name

Learn more about the data here

Interpore Cross International Inc

Manufacturer Address
Interpore Cross International Inc, 181 Technology Drive, Irvine CA 92618
Source
USFDA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)