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Ortek Therapeutics, Inc.

ORTEK THERAPEUTICS, INC · Model Ortek-ECD · UDI-DI 00858197004062

NBLLFC
1
510(k) clearances
6
Adverse events
0
Recalls
19
Facilities

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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.