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Cellulize

PHOTONICA USA, LLC · Model 60002 · UDI-DI 00860925000314

OLI Prescription
1
510(k) clearances
16
Adverse events
3
Recalls
16
Facilities

Description

Cellulize, Green Light (532nm)

Recalls

DateFirmReason
2014-05-06Advanced Photonic Systems, LLCMarketing without marketing clearance or approval.
2014-05-06Advanced Photonic Systems, LLCMarketing without marketing clearance or approval.
2014-05-06Advanced Photonic Systems, LLCMarketing without marketing clearance or approval.

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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.