# Cambridge Endoscopic Devices

- Location (FDA's records): Marlborough, MA
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)

## Firms that cite its devices most
- Lumendi, LLC: 1 (https://510kreport.com/company/lumendi)
- Steerable Technologix: 1 (https://510kreport.com/company/steerable-technologix)
- Human Extension, Ltd.: 1 (https://510kreport.com/company/human-extension)
- Dex Surgical: 1 (https://510kreport.com/company/dex-surgical)
- Kinetic Surgical, LLC: 1 (https://510kreport.com/company/kinetic-surgical)

## Its most-cited devices
- K061425: Purewrist Scissors, Model PW1101-01;Purewrist Dissector,  Model PW1201-01;Purewrist Hook, Model PW1301-01 (2006), cited by 5

## Recent decisions
- K061425: Purewrist Scissors, Model PW1101-01;Purewrist Dissector,  Model PW1201-01;Purewrist Hook, Model PW1301-01 (Aug 10, 2006)

Source page: https://510kreport.com/company/cambridge-endoscopic-devices