FDA Device Intelligence
Home › Philips Ds North America LLC › Invivo

Invivo

Philips Ds North America LLC · Model 98960320328 · UDI-DI 00884838072763

MIG
2
510(k) clearances
3
Adverse events
0
Recalls
6
Facilities

Description

LeLoc Double Hook Wire Loc. Needle

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.