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
1309021233
Device Listing 1309021233
Listing Summary
#
Listing key
1309021233
Premarket submission
K172662
Device
reVive Perioral
Applicant
Led Technologies, Inc.
Product code
OHS
Decision date
2018-01-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
235146
3015974280
3012420078
LED TECHNOLOGIES, INC.
1
Y
2026-01-01
11701 Belcher Rd S., Suite 110 Largo FL US 33773