FDA Device Intelligence
Home › SKLAR CORPORATION › Sklar®

Sklar®

SKLAR CORPORATION · Model 90-5260 · UDI-DI 30649111061916

HDX
1
510(k) clearances
4
Adverse events
1
Recalls
19
Facilities

Description

SILICONE VAG DILATORS ST/4 SML

Recalls

DateFirmReason
2015-06-19CooperSurgical, Inc.Incorrect expiration date on outer carton kit label

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.