FDA applicant
Joint Medical Products Corp.
FDA records 33 decisions for Joint Medical Products Corp. (Stamford, CT) from 1984 to 1996: 33 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and JWH (Prosthesis, Knee, Patellofemorotibial…). 6 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Joint Medical Products Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Joint Medical Products Corp. since 2007.
Recalls per year
6in 2014
Class I Class II/III not classified
Planning a device like Joint Medical Products Corp.’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 “Joint”
FDA records each applicant name separately; these may or may not be the same firm.