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
1681808333
Device Listing 1681808333
Listing Summary
#
Listing key
1681808333
Premarket submission
K990561
Device
OPTICAL FORCEPS
Applicant
Pilling Weck Surgical
Product code
JEK
Decision date
1999-05-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
152269
3010041511
3010041511
Teleflex LLC (NADC)
1
Y
2026-01-01
11245 N Distribution Cove Olive Branch MS US 38654
174940
3010089057
3010089057
Teleflex Medical Tuttlingen GmbH
1
N
2020-04-25
Kaufgasse 1 Wurmlingen Baden-Wurttemberg DE 78573
175463
3011137372
3005747797
Teleflex Medical LLC
1
Y
2026-01-01
3015 Carrington Mill Blvd Morrisville NC US 27560