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
1683941561
Device Listing 1683941561
Listing Summary
#
Listing key
1683941561
Premarket submission
K240615
Device
Leos Laser and Endoscopy System
Applicant
Beaver-Visitec International, Inc.
Product code
HQF
Decision date
2025-04-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
120002
1211998
1211998
Beaver-Visitec International, Inc.
1
Y
2026-01-01
303 Wyman St Ste 350 Waltham MA US 02451