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
1838842058
Device Listing 1838842058
Listing Summary
#
Listing key
1838842058
Premarket submission
K213606
Device
EvoEndo Single-Use Endoscopy System
Applicant
EvoEndo, Inc.
Product code
FDS
Decision date
2022-02-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
302791
3021691063
3021691063
EVOENDO, INC.
1
N
2026-01-01
888 E Belvidere Rd Ste 212 Grayslake IL US 60030