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Symmetry Surgical

ASPEN SURGICAL PRODUCTS, INC. · Model 73-48-30 · UDI-DI 00887482124109

KAI Prescription
9
510(k) clearances
4
Adverse events
1
Recalls
109
Facilities

Description

Symmetry® Mirror; Laryngeal; #9; 8 3/4 in

Recalls

DateFirmReason
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

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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.