Data / Medical devices / Brush, Dermabrasion, Manual / United States
FDA-registered makers of Brush, Dermabrasion, Manual in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Brush, Dermabrasion, Manual (product code GED). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Brush, Dermabrasion, Manual
- Product code
- GED
- Country
- United States
Makers of Brush, Dermabrasion, Manual in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bel-Med, Inc | Mount Vernon, WA, United States | Specification developer | 1 | July 28, 1982 | 0 | 0 | 0 | api.fda.gov |
| Avalign Instruments & Implants | Fort Wayne, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioseal | Placentia, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Spencer, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danelli Ocular Creations LLC | Mishawaka, IN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Evoskin LLC | Burlington, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| FridaBaby LLC | Miami, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LH Medical Corporation | Fort Wayne, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luxene Beauty | Kaysville, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meddux Development Corporation LLC | Boulder, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Millstone Medical Outsourcing LLC | Olive Branch, MS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R2 Technologies, Inc. | Dublin, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wethrivv LLC | New Hope, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.