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Data / Medical devices / Brush, Dermabrasion, Powered / United States

FDA-registered makers of Brush, Dermabrasion, Powered in the United States: 33 establishments

33 establishments in the United States are registered with the FDA to make Brush, Dermabrasion, Powered (product code GFE). 0 have 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, Powered
Product code
GFE
Country
United States

Makers of Brush, Dermabrasion, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
360 Aesthetic Devices, LLCNaples, FL, United StatesSpecification developer0000api.fda.gov
Advance-Esthetic LLCFort Lauderdale, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Alleva Medical DevicesPomona, CA, United StatesManufacturer0000api.fda.gov
Amarigo IncLos Angeles, CA, United StatesManufacturer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Brera Medical IncorporatedNorthborough, MA, United StatesManufacturer0000api.fda.gov
CPMT Laser Usa LLCMiami, FL, United StatesManufacturer0000api.fda.gov
Candela CorporationMarlborough, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Genesis Biosystems Inc.Lewisville, TX, United StatesManufacturer0000api.fda.gov
Global TV Concepts, Ltd.Coconut Creek, FL, United StatesSpecification developer0000api.fda.gov
Glownar Aesthetics. LLCDavie, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Hatch Product Development LLCWauconda, IL, United StatesContract manufacturer0000api.fda.gov
Heat In A Click LLCDania, FL, United StatesSpecification developer0000api.fda.gov
Hi Tech Electronic Manufacturing CorporationOceanside, CA, United StatesContract manufacturer0000api.fda.gov
HydraFacial LLCLong Beach, CA, United StatesManufacturer0000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
Lifeline Medical, Inc.Mount Dora, FL, United StatesManufacturer0000api.fda.gov
MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA CellmyxCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
Neauvia North America, IncRaleigh, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesContract manufacturer0000api.fda.gov
Precision Edge Surgical Products CompanySault Sainte Marie, MI, United StatesContract manufacturer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesSpecification developer0000api.fda.gov
Procell Therapies, LLCAustin, TX, United StatesManufacturer0000api.fda.gov
Raja Trading Company, Inc.Fairfax, VA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Rejuvatek Medical, IncSandy, UT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
TG3 ElectronicsKenosha, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
XOD IncPhiladelphia, PA, United StatesSpecification developer0000api.fda.gov
Xsonx, LLCCharlotte, NC, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Zeltiq Aesthetics Inc.Dublin, CA, United StatesManufacturer0000api.fda.gov
Zeltiq Aesthetics, Inc.Pleasanton, CA, United StatesSpecification developer0000api.fda.gov
Zeltiq Aesthetics, Inc.Livermore, CA, United StatesManufacturer0000api.fda.gov
Zeltiq Aesthetics IncDublin, CA, United StatesManufacturer0000api.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.