Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1672703840
Device Listing 1672703840
Listing Summary
#
Listing key
1672703840
Premarket submission
K230272
Device
Renuvion® APR Handpiece
Applicant
Apyx Medical Corporation
Product code
GEI
Decision date
2023-04-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
102771
3007593903
3007593903
Apyx Medical Corporation
1
Y
2026-01-01
5115 Ulmerton Rd Clearwater FL US 33760