Data / Medical devices / Retractor, All Types

Retractor, All Types (EIG): 247 FDA-registered makers in 19 countries

247 establishments in 19 countries are registered with the FDA to make Retractor, All Types (product code EIG, Class 1, 21 CFR 872.4565). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on June 3, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

EIG

Device class

1

Regulation

872.4565

Medical specialty

Dental

Makers by country

Makers of Retractor, All Types

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 June 3, 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.