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Data / Medical devices / Table, Obstetrical, Ac-Powered (And Accessories)

Table, Obstetrical, Ac-Powered (And Accessories) (HDD): 11 FDA-registered makers in 6 countries

11 establishments in 6 countries are registered with the FDA to make Table, Obstetrical, Ac-Powered (And Accessories) (product code HDD, Class 2, 21 CFR 884.4900). 1 of them has a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 7 510(k) clearances under this code, the latest on October 16, 1995, and lists 6 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
HDD
Device class
2
Regulation
884.4900
Medical specialty
Obstetrics/Gynecology

Makers by country

CountryMakers
United States3
China3
India2
Vietnam1
South Korea1
Czechia1

Makers of Table, Obstetrical, Ac-Powered (And Accessories)

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
Stryker MedicalPortage, MI, United StatesManufacturer, Specification developer1October 16, 1995020api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer0000api.fda.gov
Geeken Seating Collection Private LimitedGURGAON Haryana, IndiaManufacturer0000api.fda.gov
Hebei Jiede Medical Equipment Co., Ltd.Hengshui Hebei, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Hoang Nguyen Health Services Equipment Manufacture And Trading Company LimitedLy Thuong Kiet Ward Ninh Binh, VietnamManufacturer0000api.fda.gov
Kanghui Medical Technology (suzhou) Co.,ltdSuzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Lemon Co., LtdGumi-si Gyeongbuk, South KoreaManufacturer0000api.fda.gov
LINET spol. s r.o.Slany Stredocesky Kraj, CzechiaManufacturer0010api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
Ningbo Just Soon Industrial LimitedNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
Paras Surgico FactoryDelhi, IndiaManufacturer0000api.fda.gov

Updated October 16, 1995. 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.