# Urogyn, Ltd.

- Location (FDA's records): Natick, MA
- FDA decisions: 2 (2000–2002): 2 510(k) clearances
- Product codes: KNA (2)
- Predicates its devices cite: 0 (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

## Recent decisions
- K014248: DND 202 Manual Urological Digital Needle Driver (Mar 21, 2002)
- K001590: DND 101 (Aug 2, 2000)

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