FDA applicant
Johnson & Johnson Orthopaedics, Inc.
FDA records 22 decisions for Johnson & Johnson Orthopaedics, Inc. (Raynham, MA) from 1990 to 1994: 22 510(k) clearances. Most are in product codes JWH (Prosthesis, Knee, Patellofemorotibial…) and LZO (Prosthesis, Hip, Semi-Constrained…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Johnson & Johnson Orthopaedics, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Johnson & Johnson Orthopaedics, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Johnson & Johnson Orthopaedics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Johnson”
FDA records each applicant name separately; these may or may not be the same firm.