# Ntero Surgical, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 3 (1999–2002): 3 510(k) clearances
- Product codes: GEI (3)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 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
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Surgical Laser Technologies, Inc.: 1 (https://510kreport.com/company/surgical-laser-technologies)
- Dorsal Orthopedic Corp.: 1 (https://510kreport.com/company/dorsal-orthopedic)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Vnus Medical Technologies, Inc.: 1 (https://510kreport.com/company/vnus-medical-technologies)

## Its most-cited devices
- K992572: Ntero RF Sleeve (1999), cited by 1

## Recent decisions
- K014251: Ntero Hotrod System (Mar 26, 2002)
- K010815: Ntero Nomad System (Jun 15, 2001)
- K992572: Ntero RF Sleeve (Sep 24, 1999)

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