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NEW ORLEANS LENS LOOP
SONTEC INSTRUMENTS, INC. · Model 12-4330 · UDI-DI 00192896013483
HND
Prescription
6
510(k) clearances
91
Adverse events
0
Recalls
163
Facilities
Description
NEW ORLEANS LENS LOOP SINGLE ENDED
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Get your free API keyRead the docsData 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.