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Data / Medical devices / Screw, Fibroid, Gynecological

Screw, Fibroid, Gynecological (HHO): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Screw, Fibroid, Gynecological (product code HHO, Class 2, 21 CFR 884.4530). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on May 18, 1992, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
HHO
Device class
2
Regulation
884.4530
Medical specialty
Obstetrics/Gynecology

Makers by country

CountryMakers
United States2
Germany1

Makers of Screw, Fibroid, Gynecological

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
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer1May 18, 1992000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer1May 18, 1992000api.fda.gov
Gimmi GMBHTUTTLINGEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov

Updated May 18, 1992. 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.