Home › The Brewer Company LLC › Versa Exam Table
Versa Exam Table
The Brewer Company LLC · Model 1000 · UDI-DI 00728564010005
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
| Date | Firm | Reason |
|---|---|---|
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical 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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
