Data / Medical devices / Brush, Biopsy, General & Plastic Surgery / United States
FDA-registered makers of Brush, Biopsy, General & Plastic Surgery in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Brush, Biopsy, General & Plastic Surgery (product code GEE). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Brush, Biopsy, General & Plastic Surgery
- Product code
- GEE
- Country
- United States
Makers of Brush, Biopsy, General & Plastic Surgery in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Conmed Corporation | Westborough, MA, United States | Specification developer | 1 | March 5, 1982 | 0 | 0 | 0 | api.fda.gov |
| Autocam Medical | Murfreesboro, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Elmed, Inc. | Glendale Heights, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Endo-Therapeutics, Inc. | Clearwater, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gsource, LLC. | Emerson, NJ, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Histologics LLC | Anaheim, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hobbs Medical, Inc. | Stafford Springs, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medgyn Products, Inc. | Westmont, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Packaging Corporation | Camarillo, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.