# Medicon Instruments, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 6 (1994–1994): 6 510(k) clearances
- Product codes: GCJ (3), GEI (2), DRC (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
- K936246: Medicon Instruments Bipolar Forcepts and Electrodes (Jul 21, 1994)
- K936249: Medicon Instruments Unipolar Coagulation Electrodes (Jul 21, 1994)
- K936262: Dissectors, Forceps, Scissors, Dilation Sets, and Gall Stone Collectors (Jul 1, 1994)
- K936247: Medicon Instruments Trocars, Trocar Sleeves and Reduction Sleeves (May 19, 1994)
- K936248: Medicon Instruments Cholangiography Needles, Guide Tubes, Injection Needles, Verres Insufflation Needles and Holders (May 16, 1994)
- K936250: Retractors, Speculum, Clip Applier for Titanium Clips, 2-Way Stop Cock, Palpation Probe, Knot Guide, Roeder Loop (May 12, 1994)

Source page: https://510kreport.com/company/medicon-instruments