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
1713446908
Device Listing 1713446908
Listing Summary
#
Listing key
1713446908
Premarket submission
K121471
Device
LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS
Applicant
Lightscalpel, LLC
Product code
GEX
Decision date
2012-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
120444
3008720474
3008720474
LIGHTSCALPEL INC
1
N
2026-01-01
11818 North Creek Parkway N, Suite 100 Bothell WA US 98011