FDA Device Intelligence
Home › ASPEN SURGICAL PRODUCTS, INC. › Symmetry Quickert

Symmetry Quickert

ASPEN SURGICAL PRODUCTS, INC. · Model 60-2111 · UDI-DI 00887482111567

HNL Prescription
10
510(k) clearances
40
Adverse events
1
Recalls
155
Facilities

Description

Symmetry® Probe, Quickert Lacrimal Intubation, #1

Recalls

DateFirmReason
2015-02-26Quest Medical, Inc.Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels

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 docs
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.