FDA Device Intelligence
HomeNOVO SURGICAL, INC. › Novo Surgical Inc.

Novo Surgical Inc.

NOVO SURGICAL, INC. · Model E97486-21 · UDI-DI 00842331176159

KAP Prescription
1
510(k) clearances
5
Adverse events
0
Recalls
95
Facilities

Description

zenith antrum curette, 7 1/2" (19.0 cm), 1.5 mm x 6.0 mm cup, angled up

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.