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Data / Medical devices / Chair, Surgical, Ac-Powered

Chair, Surgical, Ac-Powered (GBB): 37 FDA-registered makers in 17 countries

37 establishments in 17 countries are registered with the FDA to make Chair, Surgical, Ac-Powered (product code GBB, Class 1, 21 CFR 878.4960). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on December 5, 1996, and lists 1 recall event (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
GBB
Device class
1
Regulation
878.4960
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
United States12
Germany5
China2
Brazil2
India2
South Korea2
Japan2
Hungary1
Turkey1
Taiwan1
Mexico1
Australia1
Spain1
Israel1
Sweden1
Canada1
Italy1

Makers of Chair, Surgical, Ac-Powered

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
Atmos Medizintechnik GMBH & Co. KGLENZKIRCH Baden-Wurttemberg, GermanyExporter to the US, Manufacturer0000api.fda.gov
BRUMABA GmbH & Co.KGGeretsried Bavaria, GermanyManufacturer0000api.fda.gov
Champion MFG, INC.Ocala, FL, United StatesManufacturer0010api.fda.gov
DentronicSan Leandro, CA, United StatesManufacturer0000api.fda.gov
Dexta Corp.Napa, CA, United StatesManufacturer0000api.fda.gov
Digiterm Ltd.Gyongyos Heves, HungaryManufacturer0000api.fda.gov
Foshan Any Home Care Medical Technology Co.,ltd.Foshan Guangdong, ChinaManufacturer0000api.fda.gov
GF Health Products, IncAtlanta, GA, United StatesManufacturer, Specification developer0000api.fda.gov
GF Health Products, Inc.Fond du Lac, WI, United StatesManufacturer0000api.fda.gov
Gokler GroupSivas, TurkeyManufacturer0000api.fda.gov
Happersberger Otopront GMBHHohenstein Hesse, GermanyManufacturer0000api.fda.gov
Hellstern Medical GMBHWannweil Baden-Wurttemberg, GermanyComplaint file establishment, Exporter to the US, Specification developer0000api.fda.gov
High Spot Health Technology Co., Ltd.Taichung City, TaiwanContract manufacturer0000api.fda.gov
Huangshan Jinfu Medical Equipment Co., Ltd.Huangshan City Anhui, ChinaManufacturer0000api.fda.gov
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov
JEDMED Instrument CompanySaint Louis, MO, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Knu, LLCLeland, MS, United StatesManufacturer0000api.fda.gov
Knu, LLCCannelton, IN, United StatesManufacturer0000api.fda.gov
Medical Technology Industries, Inc.Salt Lake City, UT, United StatesManufacturer0000api.fda.gov
Medpej Equipamentos Medicos LtdaRibeirao Preto Sao Paulo, BrazilManufacturer0000api.fda.gov
Midmark CorporationVersailles, OH, United StatesManufacturer0000api.fda.gov
Myvision Medical Pvt. Ltd.Ahmedabad Gujarat, IndiaManufacturer0000api.fda.gov
MegaGen Implant Co., Ltd. (Secheon 2nd factory)Daegu, South KoreaManufacturer0000api.fda.gov
Modsel Pty LtdMARYBOROUGH Queensland, AustraliaManufacturer0000api.fda.gov
Olsen Industria E Comercio S/APalhoca Santa Catarina, BrazilManufacturer0000api.fda.gov
Optomic Espana, S.A.COLMENAR VIEJO Madrid(Province), SpainManufacturer0000api.fda.gov
Restand MedicZur Yigal Central, IsraelManufacturer0000api.fda.gov
Rini Ergoteknik ABVallentuna Uppsala, SwedenManufacturer0000api.fda.gov
Samsung Medison Co., Ltd.HONGCHEON-GUN Gangwon, South KoreaManufacturer0000api.fda.gov
SCHMITZ medical GmbHWickede North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
Schuerch CorporationAbington, MA, United StatesManufacturer0000api.fda.gov
Silhouet-Tone CorporationLAVAL Quebec, CanadaComplaint file establishment, Manufacturer0000api.fda.gov
Smart Step Surgical, LLCBillings, MT, United StatesSpecification developer0000api.fda.gov
Takara Belmont CorporationOsaka, JapanComplaint file establishment, Specification developer0000api.fda.gov
Takara Belmont Corporation,shiga Equipment FactoryKONAN Shiga, JapanComplaint file establishment, Manufacturer0000api.fda.gov
Tecnodent SRLCasalecchio di Reno Bologna, ItalyManufacturer0000api.fda.gov
United Poly Engineering Pvt. Ltd.New Delhi, IndiaManufacturer0000api.fda.gov

Updated December 5, 1996. 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.