FDA Device Intelligence
HomeNICO CORPORATION › NICO Myriad-LX

NICO Myriad-LX

NICO CORPORATION · Model NN-7064 · UDI-DI 00816744027643

FSSFTD Prescription
1
510(k) clearances
118
Adverse events
0
Recalls
38
Facilities

Description

Light Source - Analog

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.