FDA Device Intelligence
Home › BBig B.V. › BBIG

BBIG

BBig B.V. · Model F21639382 · UDI-DI 08719616019451

HQZ
10
510(k) clearances
35
Adverse events
1
Recalls
1,111
Facilities

Description

F21639382

Recalls

DateFirmReason
2003-05-02Magnivision, Inc.Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.

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.