FDA Device Intelligence
Home › HNM STAINLESS, LLC. › HNM MEDICAL

HNM MEDICAL

HNM STAINLESS, LLC. · Model HNM-1-61-0377 · UDI-DI 00842962145302

JYO
7
510(k) clearances
7
Adverse events
1
Recalls
80
Facilities

Description

HOUSE LANCET KNIFE, 6 1/2", 2MMX3MM BLADE, #2, ANG 45°

Recalls

DateFirmReason
2013-03-27Summit Medical, Inc.Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong blade. The box contains Myringotomy Spear Blade (Juvenile).

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.