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Data / Medical devices / Table, Surgical With Orthopedic Accessories, Manual

Table, Surgical With Orthopedic Accessories, Manual (JEB): 35 FDA-registered makers in 8 countries

35 establishments in 8 countries are registered with the FDA to make Table, Surgical With Orthopedic Accessories, Manual (product code JEB, Class 1, 21 CFR 878.4950). 1 of them has a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 13 510(k) clearances under this code, the latest on March 6, 1991, and lists 7 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
JEB
Device class
1
Regulation
878.4950
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
United States20
India4
China3
Germany3
Taiwan2
France1
Mexico1
Switzerland1

Makers of Table, Surgical With Orthopedic Accessories, Manual

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
Steris CorporationMontgomery, AL, United StatesComplaint file establishment, Manufacturer1March 6, 1991000api.fda.gov
A.M. Surgical, Inc.Nashua, NH, United StatesSpecification developer0000api.fda.gov
American Benchmark Machine WorksOlympia, WA, United StatesContract manufacturer0000api.fda.gov
AmplitudeValence Drome, FranceComplaint file establishment, Manufacturer0000api.fda.gov
Arthro-Positioning Systems LLCBogart, GA, United StatesManufacturer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
B & J Medical LLCKendallville, IN, United StatesContract manufacturer0000api.fda.gov
Biomet, Inc.Warsaw, IN, United StatesManufacturer0010api.fda.gov
Chengdu Ruinuo Meijer Medical Instrument Co., Ltd.Chengdu Sichuan, ChinaManufacturer0000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesManufacturer, Specification developer0000api.fda.gov
Depuy Spine, Inc.Raynham, MA, United StatesSpecification developer0000api.fda.gov
DePuy Mitek, Inc.Raynham, MA, United StatesSpecification developer0000api.fda.gov
Domico Med-Device, LLCFenton, MI, United StatesContract manufacturer0000api.fda.gov
Galaxy IndiaNew Delhi, IndiaManufacturer0000api.fda.gov
General Hospital Supply Corp.Indian Trail, NC, United StatesSpecification developer0000api.fda.gov
Globus Medical, Inc.Audubon, PA, United StatesManufacturer0000api.fda.gov
Guenter Stoffel Medizintechnik GMBHWURMLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Hebei Ruinuo Medical Instrument Co LtdShijiazhuang Hebei, ChinaManufacturer0000api.fda.gov
Innomed, Inc.Savannah, GA, United StatesSpecification developer0000api.fda.gov
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KGLIPTINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Jorg & Sohn GMBHAhorn-Schorkendorf Bavaria, GermanyExporter to the US, Manufacturer0000api.fda.gov
Mammon International Corp.Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Match Grade MedicalNeenah, WI, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer0000api.fda.gov
Orthopediatrics, CorpWarsaw, IN, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesManufacturer0000api.fda.gov
Syntec Scientific Corp.CHANG HUA Changhua, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Shanghai PAX Medical Instrument Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
United Medi Equip Private LimitedNew Delhi, IndiaManufacturer0000api.fda.gov
United Poly Engineering Pvt. Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
United Surgical IndustriesSAHIBABAD Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Viant Medical, LLCFort Wayne, IN, United StatesContract manufacturer0000api.fda.gov
White Surgical, Inc.Fort Wayne, IN, United StatesManufacturer, Specification developer0000api.fda.gov

Updated March 6, 1991. 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.