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Versa Exam Table

The Brewer Company LLC · Model 1000 · UDI-DI 00728564010005

FRK
4
510(k) clearances
652
Adverse events (1 deaths)
1
Recalls
69
Facilities

Description

Versa products will be sold into the physician office market and are intended to be used by healthcare professionals employed by physician offices, medical clinics, and IDNs. Versa products will be used to examine a wide variety of patients of various sizes and mobility. Versa will be used inside of an office/clinic and require no special environmental needs.

Recalls

DateFirmReason
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.