# Techmedica, Inc.

- Location (FDA's records): Camarillo, CA
- FDA decisions: 31 (1982–1994): 31 510(k) clearances
- Product codes: JWH (5), HRS (3), KWY (2), LZO (2), HWC (2), HSX (2), JDI (1), DZJ (1), JDR (1), JDL (1), FZX (1), HWE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 12 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bioplate, Inc.: 4 (https://510kreport.com/company/bioplate)
- Zimmer, Inc.: 3 (https://510kreport.com/company/zimmer)
- Howmedica Corp.: 3 (https://510kreport.com/company/howmedica)
- Bionx Implants, Inc.: 1 (https://510kreport.com/company/bionx-implants)
- Imaging Therapeutics, Inc.: 1 (https://510kreport.com/company/imaging-therapeutics)

## Its most-cited devices
- K921458: TMP Microplating System (1992), cited by 4
- K921801: Modification Techmedica MP (Miniplating) System (1992), cited by 4
- K911058: Techmedica Cad/Cam Custom Hip (1993), cited by 1
- K914072: Continuum Knee System (CKS) (1992), cited by 1
- K896542: Addition to the Continuum Knee System (CKS (TM)) (1990), cited by 1
- K903286: Continuum Knee System (CKS)-Modification (1990), cited by 1

## Recent decisions
- K933935: CKS Porous Coated Femoral Component (Oct 11, 1994)
- K932017: Techmedica Continuum Hip with HA Coating (Sep 1, 1994)
- K931929: Techmedica Continuum Hip System (Mar 29, 1994)
- K926387: Techmedica Standard Cemented Hip System (Feb 1, 1994)
- K925420: Techmedica Standard Bipolar System (Sep 28, 1993)
- K923808: Muller Straight Stem Femoral Prosthesis (Jul 27, 1993)
- K926579: Techmedica 6.5MM Self-Tapping Cancellous Bone Scre (Apr 6, 1993)
- K911058: Techmedica Cad/Cam Custom Hip (Feb 23, 1993)

Source page: https://510kreport.com/company/techmedica