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
1174458313
Device Listing 1174458313
Listing Summary
#
Listing key
1174458313
Premarket submission
K201001
Device
Modulith SLX-F2
Applicant
Karl Storz Endoscopy America
Product code
LNS
Decision date
2021-03-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
313975
1061158
1000511585
STORZ MEDICAL AMERICA, INC.
1
Y
2026-01-01
1000 COBB PLACE BLVD BUILDING 400, SUITE 450 Kennesaw GA US 30144
16839
9613347
3002808188
STORZ MEDICAL AG
1
N
2026-01-01
LOHSTAMPFESTRASSE 8 TAEGERWILEN Thurgau CH 8274