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HAI Spatula

Hightech American Industrial Labs Inc · Model 1 · UDI-DI 00852194002144

HND

510(k) clearances

Adverse events

Recalls

161

Facilities

Description

Spatula, Surgical instrument for ophthalmic use

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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.