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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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