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Photonica Professional

PHOTONICA USA, LLC · Model 60001 · UDI-DI 00860925000307

OLIGEX Prescription
10
510(k) clearances
16
Adverse events
3
Recalls
15
Facilities

Description

Photonica Professional, Red Light (635 nm)

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.