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Data / Medical devices / Epilator, High Frequency, Tweezer-Type

Epilator, High Frequency, Tweezer-Type (KCX): 28 FDA-registered makers in 5 countries

28 establishments in 5 countries are registered with the FDA to make Epilator, High Frequency, Tweezer-Type (product code KCX, Class 1, 21 CFR 878.5360). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 25 510(k) clearances under this code, the latest on December 17, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
KCX
Device class
1
Regulation
878.5360
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
Pakistan12
China10
United States4
Hong Kong1
Switzerland1

Makers of Epilator, High Frequency, Tweezer-Type

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Buraq Surgical Corp.SIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Chaplet InternationalLahore Punjab, PakistanManufacturer0000api.fda.gov
Cole InstrumentsAlpharetta, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Comfort Surgical InstrumentsSialkot Punjab, PakistanManufacturer0000api.fda.gov
Crimson InternationalSialkot Punjab, PakistanManufacturer0000api.fda.gov
Dongguan Yibiao Electronic Technology Co.,ltdDong Guan City Guangdong, ChinaManufacturer0000api.fda.gov
DayOn Daily Chemical Co., LtdYangzhou Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Ever Strong Manufacturing LtdDongguan Guangdong, ChinaManufacturer0000api.fda.gov
Foshan CICADA Dental Instrument Co., Ltd.Foshan Guangdong, ChinaManufacturer0000api.fda.gov
Global TV Concepts, Ltd.Coconut Creek, FL, United StatesSpecification developer0000api.fda.gov
Golden Aim International LtdShenzhen City,, GUANGDONG, CHINA, Hong KongContract manufacturer0000api.fda.gov
Guangdong Comfort Medical Products Co., Ltd.Jiangmen Guangdong, ChinaManufacturer0000api.fda.gov
Lianyungang Brilliant Industrial Co., Ltd.LIANYUNGANG Jiangsu, ChinaContract manufacturer0000api.fda.gov
Manufactures D'outils Dumont S.A.MONTIGNEZ Jura, SwitzerlandManufacturer0000api.fda.gov
Medcave Private LimitedSialkot Punjab, PakistanManufacturer0000api.fda.gov
Meed Skills SurgicalSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Nextcon InternationalSialkot Punjab, PakistanContract manufacturer, Manufacturer0000api.fda.gov
Orthopli Corp.Philadelphia, PA, United StatesManufacturer0000api.fda.gov
Oogie Solutions LLCPotomac, MD, United StatesManufacturer0000api.fda.gov
S.G. ManufacturersSialkot Punjab, PakistanManufacturer0000api.fda.gov
Shenzhen Eyco Technology Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Rogin Medical Co., Ltdshenzhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Spartech Instruments & Co.Sialkot, Punjab, PakistanExporter to the US, Manufacturer0000api.fda.gov
Technimen SkillersSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Ultra Surgical (pvt.) LtdSIALKOT Punjab, PakistanManufacturer0000api.fda.gov
Volgo Care International (private) LimitedSialkot Punjab, PakistanContract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Yuhuan City Shengbo Mould Manufacturing Co.,Ltd.Yuhuan Zhejiang, ChinaManufacturer0000api.fda.gov
Zhongshan Kingdom Electrical Appliance Co., Ltd.Zhongshan Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated December 17, 1997. 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.