# Adven Medical

- Location (FDA's records): Lubbock, TX
- FDA decisions: 6 (1994–2002): 6 510(k) clearances
- Product codes: HWE (2), JOW (2), KBG (1), GFA (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 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
- Smith & Nephew Dyonics, Inc.: 1 (https://510kreport.com/company/smith-nephew-dyonics)
- The Kendal Co.: 1 (https://510kreport.com/company/kendal)

## Recent decisions
- K021528: Reprocessed Venodyne Sequential Compression Sleeves / Wrap (Aug 21, 2002)
- K013987: Reprocessed Disposable Trocars (Mar 1, 2002)
- K012675: Reprocessed Used Disposable Sequential Compression Sleeves/Wraps (Feb 12, 2002)
- K012694: Reprocessed Used Disposable Arthroscopic Blades and Burs (Feb 4, 2002)
- K012676: Reprocessed Used, Disposable Blades, Burs, Bits and Taps (Feb 4, 2002)
- K940501: RE-Sharpenable Saw Blades (Jun 28, 1994)

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