FDA applicant
Techmedica, Inc.
FDA records 31 decisions for Techmedica, Inc. (Camarillo, CA) from 1982 to 1994: 31 510(k) clearances. Most are in product codes JWH (Prosthesis, Knee, Patellofemorotibial…) and HRS (Plate, Fixation, Bone). 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 Techmedica, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Techmedica, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Techmedica, 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) Report