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
1024229177
Device Listing 1024229177
Listing Summary
#
Listing key
1024229177
Premarket submission
K963901
Device
ELECTROSURGICAL PROBE
Applicant
Smith & Nephew Endoscopy, Inc.
Product code
GEI
Decision date
1996-11-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
149131
1219602
1219602
SMITH & NEPHEW INC.
1
N
2026-01-01
ENDOSCOPY 120 FORBES BLVD. SUITE 150 / 130 FORBES BLVD. MANSFIELD MA US 02048
149134
1643264
1643264
SMITH & NEPHEW INC.
1
Y
2026-01-01
ENDOSCOPY 76 S. MERIDIAN AVE. OKLAHOMA CITY OK US 73107
149135
3003604053
3003604053
SMITH & NEPHEW INC.
1
N
2026-01-01
ENDOSCOPY 150 Minuteman Rd ANDOVER MA US 01810