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Manufacturers
DePuy Orthopaedics, Inc.
Manufacturer Address
DePuy Orthopaedics, Inc., 325 Paramount Dr, Raynham MA 02767-5199
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA
2 Events
Recall of Device Recall Concorde Lift
Recall of Device Recall Concorde Lift
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2 devices in the database
Device Recall Concorde Lift
Model / Serial
Product code: 287804102 Lot number: 122315-B R, 122315-A R, 041117A
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
Concorde Lift Torque Limiting Handle. || Must be used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Device Recall Concorde Lift
Model / Serial
Product code: 287804101G Lot number: 052316-A R, 121416-A R
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution
Product Description
Concorde Lift Driver Shaft AO. || Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
11 manufacturers with a similar name
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DePuy Orthopaedics, Inc.
Manufacturer Address
DePuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA
Depuy Orthopaedics, Inc.
Manufacturer Address
Depuy Orthopaedics, Inc., 700 Orthopaedic Drive, Warsaw IN 46581
Source
USFDA
Depuy Orthopaedics, Inc.
Manufacturer Address
Depuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
Source
USFDA
DePuy Orthopaedics, Inc.
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
AMPMDRS
DePuy Orthopaedics, Inc.
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
SMPA
6 more
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