# Penn Medical Devices, Inc.

- Location (FDA's records): Basking Ridge, NJ
- FDA decisions: 8 (1986–1987): 8 510(k) clearances
- Product codes: KNT (1), FAD (1), ODC (1), KOE (1), FCL (1), BTQ (1), EZN (1), FFL (1)
- 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
- K873949: Rorertazzi Nasopharyngeal Airway (Oct 20, 1987)
- K873177: Devine  (Suprapubic Sound and Guide) (Oct 14, 1987)
- K873176: Huffman Biopsy Unit (Oct 14, 1987)
- K873178: Ureteral Bulb Dilators (Sep 30, 1987)
- K871667: Ureteral Stent (Jun 10, 1987)
- K870508: Gastrointestinal Tube (May 11, 1987)
- K862729: Penn 3-Ring Handle (Oct 24, 1986)
- K862107: Penn & Olympus Ureteroscopy Guide Sheath & Dilator (Sep 11, 1986)

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