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Data / Medical devices / Cushion, Denture, Over The Counter

Cushion, Denture, Over The Counter (EHS): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Cushion, Denture, Over The Counter (product code EHS, Class 2, 21 CFR 872.3540). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on July 15, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
EHS
Device class
2
Regulation
872.3540
Medical specialty
Dental

Makers by country

CountryMakers
China2
Liechtenstein1
South Korea1

Makers of Cushion, Denture, Over The Counter

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
Anhui GREENLAND BIOTECH CO.,LTDBengbu Anhui, ChinaManufacturer0000api.fda.gov
Bonyf AGVaduz, LiechtensteinManufacturer0000api.fda.gov
One Day Dental PartnerSuncheon-si Jeonnam, South KoreaExporter to the US, Manufacturer0000api.fda.gov
Think Big Industrial Company LimitedPudong Shanghai, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated July 15, 1997. 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.