# Robert Reid, Inc.

- Location (FDA's records): Chesterland, OH
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: HSB (1), MNI (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Disc-O-Tech Medical Technologies, Ltd.: 1 (https://510kreport.com/company/disc-o-tech-medical-technologies)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Buckman Co., Inc.: 1 (https://510kreport.com/company/buckman)
- Cross Medical Products, Inc.: 1 (https://510kreport.com/company/cross-medical-products)

## Recent decisions
- K093833: Kapss Spinal System (Oct 15, 2010)
- K093089: Magnum Nail (Nov 13, 2009)

Source page: https://510kreport.com/company/robert-reid