FDA Device Intelligence
Home › SPECTRUM BRANDS, INC. › Remington

Remington

SPECTRUM BRANDS, INC. · Model IPL7510 · UDI-DI 00074590544503

ONF
1
510(k) clearances
32
Adverse events
0
Recalls
98
Facilities

Description

Intense Pulse Light OTC hair removal device

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.