# Medron, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 3 (1994–2020): 3 510(k) clearances
- Names in FDA's records: Medron, Inc. (2); Medron, LLC (1)
- Product codes: DRE (1), LFK (1), FOZ (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
- Medcomp ( Medical Components): 1 (https://510kreport.com/company/medcomp-medical-components)
- Akcess Medical Products, Inc.: 1 (https://510kreport.com/company/akcess-medical-products)

## Recent decisions
- K192283: MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator (May 6, 2020)
- K971897: Continuous Arteriovenous Hemofiltration Catheter 10 FR (Cavh) (Oct 21, 1997)
- K940775: Injection Cap (Jun 15, 1994)

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