# Osteo AG

- Location (FDA's records): Greenwood, SC
- FDA decisions: 9 (1991–1994): 9 510(k) clearances
- Product codes: HSB (3), HTY (2), HRC (1), JDQ (1), HSZ (1), JEC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- U&I Corporation: 1 (https://510kreport.com/company/u-i)
- Osteonics Corp.: 1 (https://510kreport.com/company/osteonics)

## Its most-cited devices
- K920037: Osteo Compression Hip Screw (1992), cited by 1
- K933340: Osteo Interlocking-Compression Nail (1994), cited by 1

## Recent decisions
- K933340: Osteo Interlocking-Compression Nail (Jun 30, 1994)
- K922193: Osteo Kirschner Wire (Jul 23, 1992)
- K922196: Osteo Tibia Nail (Jul 23, 1992)
- K922195: Osteo Femoral Nail (Jul 23, 1992)
- K922194: Osteo Steinmann Pin (Jul 23, 1992)
- K920149: Osteo EX-FI-RE (Apr 9, 1992)
- K920037: Osteo Compression Hip Screw (Mar 11, 1992)
- K914374: Osteo Cerclage Wire (Dec 30, 1991)

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