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
1335837920
Device Listing 1335837920
Listing Summary
#
Listing key
1335837920
Premarket submission
K122662
Device
VERTIFLEX DIRECT DECOMPRESSION SYSTEM
Applicant
Vertiflex, Inc.
Product code
HRX
Decision date
2012-11-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
66485
3005641619
3005641619
PACIFIC INSTRUMENTS INC.
1
Y
2026-01-01
438 Hobron Lane Suite 204 Honolulu HI US 96815