510(k) Report

FDA applicant

Techmedica, Inc.

Camarillo, CA31 decisions1982–19940 recalls

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, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

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.

FIG. 1 — Techmedica, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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