# Nexmed, Inc.

- Location (FDA's records): Palm Desert, CA
- FDA decisions: 6 (1995–2004): 6 510(k) clearances
- Product codes: LPH (2), JDG (1), JDI (1), HWC (1), JWH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Alphatec/Nexmed: 1 (https://510kreport.com/company/alphatec-nexmed)

## Its most-cited devices
- K033580: Nexflex Total Hip System (2004), cited by 1

## Recent decisions
- K033580: Nexflex Total Hip System (Aug 5, 2004)
- K991882: Nexflex Total Knee System (Dec 8, 1999)
- K955171: Nexlock Femoral Stem (Feb 9, 1996)
- K955170: Nexflex Femoral Stem, Standard Design (Feb 9, 1996)
- K952629: Nexflex Total Hip System (Sep 8, 1995)
- K951656: Nexmed Cancellous Bone Screws (Jul 18, 1995)

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