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Data / Medical devices / Collimator, X-Ray

Collimator, X-Ray (EHB): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Collimator, X-Ray (product code EHB, Class 1, 21 CFR 872.1840). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on September 25, 1992, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
EHB
Device class
1
Regulation
872.1840
Medical specialty
Dental

Makers by country

CountryMakers
China3
Netherlands1

Makers of Collimator, X-Ray

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
Duphamed B.V.ALPHEN AAN DEN RIJN Zuid-Holland, NetherlandsManufacturer0000api.fda.gov
Shanghai Lions Industrial Co.,ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Shanghai Jolly Industrial Co., Ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
iBrite Suzhou Technology Co., LtdSUZHOU CITY Jiangsu, ChinaContract manufacturer0000api.fda.gov

Updated September 25, 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.