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
1023517153
Device Listing 1023517153
Listing Summary
#
Listing key
1023517153
Premarket submission
K250997
Device
Integrity™ Implant
Applicant
Anika Therapeutics, Inc.
Product code
OWX
Decision date
2025-06-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
124999
3007093114
3007093114
ANIKA THERAPEUTICS, INC.
1
Y
2026-01-01
32 Wiggins Ave Bedford MA US 01730