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
1498840024
Device Listing 1498840024
Listing Summary
#
Listing key
1498840024
Premarket submission
K210871
Device
PDO Max Suture with Dual Needle
Applicant
Pdo Max, Inc.
Product code
NEW
Decision date
2021-12-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
230972
3015289316
3015289316
PDO MAX
1
N
2026-01-01
4971 Bear Road Suite 102 Liverpool NY US 13088