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/ Neauvia North America, Inc.
Neauvia North America, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K230077
LaserME
July 17, 2023
K223222
Plasma IQ
January 17, 2023
K213261
EpilME
June 2, 2022
K212329
Plasma IQ
December 9, 2021
K202780
Sectum
July 30, 2021
K192813
Plasma IQ
March 6, 2020