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Beurer

BEURER NORTH AMERICA, L.P. · Model IPL7500 (Art.-No. 575.71) · UDI-DI 00852547004733

OHT
10
510(k) clearances
34
Adverse events (1 deaths)
0
Recalls
92
Facilities

Description

Light based, over the counter device intended for the removal of unwanted hair as well as permanent reduction in hair regrowth.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.