# Nuortho Surgical, Inc.

- Location (FDA's records): Newington, NH
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 5 (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
- Arthrocare Corp.: 1 (https://510kreport.com/company/arthrocare)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Mitek Products: 1 (https://510kreport.com/company/mitek-products)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)
- Acmi Corporation: 1 (https://510kreport.com/company/acmi)

## Recent decisions
- K101711: Ceruleau Electrosurgical Probe (Jul 1, 2010)

Source page: https://510kreport.com/company/nuortho-surgical