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Surgiform

SURGICAL TECHNOLOGY LABORATORIES INC · Model ND-03A · UDI-DI 00851988007464

FZE Prescription

510(k) clearances

211

Adverse events

Recalls

Facilities

Description

"ND-03A Nasal Dorsal Series A Silicone Implants"

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.