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
1162788442
Device Listing 1162788442
Listing Summary
#
Listing key
1162788442
Premarket submission
K213969
Device
VisionAir Patient-Specific Airway Stent
Applicant
New Cos Inc. Dba Visionair Solutions
Product code
NWA
Decision date
2022-10-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
322253
3010197296
3010197296
VisionAir Solutions
1
N
2026-01-01
1800 Triplett Blvd Akron OH US 44306