# Accutech Medical Technologies, Inc.

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 2 (2006–2009): 2 510(k) clearances
- Product codes: FFS (1), GEX (1)
- Predicates its devices cite: 10 (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
- Ceram Optec, Inc.: 3 (https://510kreport.com/company/ceram-optec)
- Lumenis, Inc.: 2 (https://510kreport.com/company/lumenis)
- Hgm, Inc.: 1 (https://510kreport.com/company/hgm)
- Cook Urological, Inc.: 1 (https://510kreport.com/company/cook-urological)
- Fibertech GmbH: 1 (https://510kreport.com/company/fibertech)
- Technology Delivery Systems, Inc.: 1 (https://510kreport.com/company/technology-delivery-systems)

## Its most-cited devices
- K061025: Accutech Endolite Probe (2006), cited by 1

## Recent decisions
- K090281: Accutech Family of Powerflex Laser Delivery Devices (Mar 4, 2009)
- K061025: Accutech Endolite Probe (May 31, 2006)

Source page: https://510kreport.com/company/accutech-medical-technologies