# Medtrex, Inc.

- Location (FDA's records): Sandy, UT
- FDA decisions: 4 (1995–1998): 4 510(k) clearances
- Product codes: GEI (4)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Aspen Laboratories, Inc.: 1 (https://510kreport.com/company/aspen-laboratories)

## Firms that cite its devices most
- Aaron Medical Industries: 2 (https://510kreport.com/company/aaron-medical-industries)
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)
- Peak Surgical, Inc.: 1 (https://510kreport.com/company/peak-surgical)

## Its most-cited devices
- K970039: Encore Electrosurgical Handcontrol Pencil (35001-001) (1997), cited by 3
- K981724: O.R.Pro 300 Electrosurgical Generator Model 40001-100 (1998), cited by 1

## Recent decisions
- K981724: O.R.Pro 300 Electrosurgical Generator Model 40001-100 (Jun 22, 1998)
- K970130: Hydrocool Dual Conductor Polymer Gel (30101-001/Corded Dispersive Electrode-Sensing (Mar 28, 1997)
- K970039: Encore Electrosurgical Handcontrol Pencil (35001-001) (Feb 26, 1997)
- K952577: Electrosurgical Dispersive Electrode (Jun 14, 1995)

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