# Medrange Corporation

- Location (FDA's records): Brea, CA
- FDA decisions: 3 (2010–2020): 3 510(k) clearances
- Names in FDA's records: Medrange Corporation (2); Medrange (1)
- Product codes: GEI (3)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 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.: 2 (https://510kreport.com/company/valleylab)
- Aspen Laboratories, Inc.: 1 (https://510kreport.com/company/aspen-laboratories)
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)
- Erbe USA, Inc.: 1 (https://510kreport.com/company/erbe-usa)

## Firms that cite its devices most
- Ascblue Corporation: 1 (https://510kreport.com/company/ascblue)

## Its most-cited devices
- K102114: Medrange Electrosurgical Generator (2010), cited by 1
- K201224: Electrosurgical Generator and Accessories (2020), cited by 1

## Recent decisions
- K201224: Electrosurgical Generator and Accessories (Sep 18, 2020)
- K122092: Medrange Electrosurgical Expansion System (Oct 23, 2012)
- K102114: Medrange Electrosurgical Generator (Nov 22, 2010)

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