# Medical Dynamics, Inc.

- Location (FDA's records): Englewood, CO
- FDA decisions: 18 (1988–1998): 18 510(k) clearances
- Product codes: HET (2), GCB (2), LQR (1), EIA (1), KGZ (1), FWH (1), FWD (1), FSW (1), FGE (1), IKO (1), FWF (1), HRX (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
- K974542: True Vision, True Vision II (Feb 17, 1998)
- K921294: Video Endoscope-Rigid Modification (Jul 20, 1994)
- K934682: Surgical Video Camera and Accessories (Feb 15, 1994)
- K930568: Adair/Veress Needle Introducer Set (Jul 22, 1993)
- K915538: Over the Wire Stone Basket (Mar 20, 1992)
- K914315: Optical Catheter Introducer Sets, Modification (Mar 4, 1992)
- K913986: Cholangiography/Cholangioscopy/Lihopaxy System (Jan 28, 1992)
- K911296: Optical Catheter Arthroscope (Sep 24, 1991)

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