# Endo Surgical Devices, Inc.

- Location (FDA's records): Hopkonton, MA
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: GEI (1), DWX (1)
- Predicates its devices cite: 1 (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

## Its most-cited devices
- K013680: Carbodissecting Endoscope (2002), cited by 1

## Recent decisions
- K020925: Carbodissecting Endoscope (Apr 29, 2003)
- K013680: Carbodissecting Endoscope (Mar 4, 2002)

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