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ADITEK
ADITEK DO BRASIL S/A · Model 09.08.9006 · UDI-DI 07899439266506
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510(k) clearances
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Adverse events
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Recalls
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Facilities
Description
Archwire Sequence Contour Niti 35° EasyClip+ Passive 14/18/14x25/16x25/17x25 w/stop w/10
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
