Data / Medical devices / Forceps, Rubber Dam Clamp

Forceps, Rubber Dam Clamp (EJG): 79 FDA-registered makers in 15 countries

79 establishments in 15 countries are registered with the FDA to make Forceps, Rubber Dam Clamp (product code EJG, Class 1, 21 CFR 872.6300). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on May 12, 1978, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code

EJG

Device class

1

Regulation

872.6300

Medical specialty

Dental

Makers by country

Makers of Forceps, Rubber Dam Clamp

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.

Updated May 12, 1978. 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.