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Data / Medical devices / Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction

Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction (PAY): 15 FDA-registered makers in 6 countries

15 establishments in 6 countries are registered with the FDA to make Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction (product code PAY, Class 2, 21 CFR 878.4420). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on January 6, 2026, 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.

Get every maker of this deviceMakers in ChinaWatch this device
Product code
PAY
Device class
2
Regulation
878.4420
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
China7
Israel4
Netherlands1
United Kingdom1
United States1
Vietnam1

Makers of Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction

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
Pollogen LtdTel Aviv, IsraelManufacturer5October 12, 2025000api.fda.gov
El Global Trade Ltd.Netanya Central, IsraelManufacturer, Specification developer2March 6, 2024000api.fda.gov
Vis (shanghai) Technology Co., Ltd.Jinshan District Shanghai, ChinaManufacturer2July 15, 2024000api.fda.gov
Endymed Medical LtdCaesarea Northern, IsraelManufacturer1December 18, 2015000api.fda.gov
Silk'n Beauty Ltd.Rotterdam Zuid-Holland, NetherlandsManufacturer1August 30, 2023000api.fda.gov
Shenzhen Lescolton Medical Equipment Co., Ltd.shenzhen Guangdong, ChinaManufacturer1June 15, 2017000api.fda.gov
The Beauty Tech Group LtdMacclesfield Cheshire East, United KingdomExporter to the US, Specification developer1March 6, 2024000api.fda.gov
Beijing Spiritlaser Science & Technology Co., Ltd.Beijing, ChinaManufacturer0000api.fda.gov
R.H. Electronics Ltd.Nof Hagalil Northern, IsraelContract manufacturer0000api.fda.gov
RH Usa, Inc.Livermore, CA, United StatesContract manufacturer0000api.fda.gov
Shenzhen Rainbow Technology Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Solex High-Tech Industries (vietnam) Company LimitedQuang Yen Town Quang Ninh, VietnamContract manufacturer0000api.fda.gov
Something High Electric (xiamen) Company Inc.Xiamen Fujian, ChinaContract manufacturer0000api.fda.gov
Shen Zhen HanShine Technology Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Xiamen Solex High-Tech Industries Co.,ltdXiamen Fujian, ChinaContract manufacturer0000api.fda.gov

Updated January 6, 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.