Home › ASPEN SURGICAL PRODUCTS, INC. › Symmetry Laborde
Symmetry Laborde
ASPEN SURGICAL PRODUCTS, INC. · Model 73-6604 · UDI-DI 00887482124130
KCG
Prescription
1
510(k) clearances
21
Adverse events (4 deaths)
1
Recalls
87
Facilities
Description
Symmetry® Dilator, Laborde Tracheal, Three-Bladed, Two Flat, One Cupped, 5 in, 125 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.
