FDA 510(k) Applications Submitted by Bio-Med USA Inc

FDA 510(k) Number Submission Date Device Name Applicant
K221789 06/21/2022 IRIS Pi Q switched Nd YAG laser Bio-Med USA Inc
K212082 07/02/2021 Picore Bio-Med USA Inc
K123710 12/04/2012 UNITOX BOTOX SYRINGE BIO-MED USA INC
K163638 12/23/2016 Dental 5 Multi Diode laser BIO-MED USA INC


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