Medrange Corporation
Brea, CA, US
Medrange Corporation appears in FDA device records in Brea, CA. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Medrange Corporation between 2010 and 2020. The busiest year on record is 2010, with 1. The most recent is 2020, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 1 |
| 2012 | 1 |
| 2020 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K201224 | Electrosurgical Generator and Accessories | GEI | Substantially Equivalent | |
| K122092 | MEDRANGE ELECTROSURGICAL EXPANSION SYSTEM | GEI | Substantially Equivalent | |
| K102114 | MEDRANGE ELECTROSURGICAL GENERATOR | GEI | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3008786200 | 3008786200 | Medrange Corporation | 480 Apollo St Ste D, Brea, CA 92821 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain