FDA Device Intelligence
Home › ELMED INCORPORATED › ELMED INCORPORATED

ELMED INCORPORATED

ELMED INCORPORATED · Model ST321604E · UDI-DI 00198506070525

HDL Prescription
2
510(k) clearances
19
Adverse events
1
Recalls
120
Facilities

Description

LASER BLACK LATERAL WALL VAGINAL RETRACTOR, GOLD PLATED RATCHET HANDLE—OPEN SHANKS—10 1/12” OVERALL LENGTH, 4 1/2” X 1” BLADE SIZE

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports 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 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.