# Diotech CO

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 2 (2014–2016): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 3 (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
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)
- Hogue Surgical, LLC: 1 (https://510kreport.com/company/hogue-surgical)

## Its most-cited devices
- K140458: Diotech Laser Fiber (2014), cited by 1

## Recent decisions
- K152667: ATOVEN-Reusable Laser Fiber (Jun 9, 2016)
- K140458: Diotech Laser Fiber (Aug 26, 2014)

Source page: https://510kreport.com/company/diotech