Home › INTEGRA LIFESCIENCES (IRELAND) LIMITED › Integra®

Integra®

INTEGRA LIFESCIENCES (IRELAND) LIMITED · Model 90542 · UDI-DI 10381780168720

FSR Prescription

510(k) clearances

100

Adverse events

Recalls

Facilities

Description

Integra® LED Headband Replacement Pads (10/Box)

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 key Read 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.