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Novo Surgical Inc.

NOVO SURGICAL, INC. · Model E7736-12 · UDI-DI 00842331168482

KAE Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

bruening septum forceps, 4 1/4" (10.8 cm) shaft, 7 3/8" (18.7 cm) overall, no. 1, 7.0 mm x 9.0 mm jaws

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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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.