# Orthoconcept, Inc.

- Location (FDA's records): Columbia, SC
- FDA decisions: 8 (1987–1994): 8 510(k) clearances
- Product codes: HRX (6), FDC (2)
- 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
- Hemodia Sas: 1 (https://510kreport.com/company/hemodia)

## Its most-cited devices
- K925160: Arthro FMS 4 (1994), cited by 1

## Recent decisions
- K925160: Arthro FMS 4 (Feb 17, 1994)
- K910164: Orthoconcept Arthroscopic Pump (Mar 27, 1991)
- K905785: Arthro-FMS-3/Irrigation Sets (Various) (Mar 26, 1991)
- K896196: Arthroscopy Disp. & Reusable Shaver Blades, Rechar (Dec 1, 1989)
- K895643: Modified Uropump* Fluid Management System (Oct 17, 1989)
- K894363: Uropump* Fluid Management System (Aug 11, 1989)
- K882469: Cordex Shaver, Blades, Recharger and Batteries (Dec 1, 1988)
- K872270: Orthoconcept Arthroscopic Pump  Orthopump (Jul 21, 1987)

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