FDA Device Intelligence
Home › SURGISTAR, INC. › SURGISTAR

SURGISTAR

SURGISTAR, INC. · Model 501030 · UDI-DI 00878799008077

BSN
9
510(k) clearances
162
Adverse events
1
Recalls
18
Facilities

Recalls

DateFirmReason
2009-11-25Millipore CorporationMembrane integrity defects may allow the passage of viable or non-viable contaminants to pass through the filter.

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 docs
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.