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
1940351877
Device Listing 1940351877
Listing Summary
#
Listing key
1940351877
Premarket submission
K162053
Device
PhotonBlade
Applicant
Invuity, Inc.
Product code
GEI
Decision date
2016-09-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
224596
3011394215
3007037347
INVUITY, INC.
1
N
2020-04-25
444 de Haro St San Francisco CA US 94107
235912
3015967359
3015967359
Stryker Instruments
1
Y
2026-01-01
1941 Stryker Way Portage MI US 49002
342047
3040335671
3040335671
Kim Wiersema
1
N
2026-01-01
1941 Stryker Way Portage MI US 49002