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
1289235775
Device Listing 1289235775
Listing Summary
#
Listing key
1289235775
Premarket submission
K991218
Device
ORATEC BIPOLAR ABLATION PROBES
Applicant
Oratec Interventions, Inc.
Product code
GEI
Decision date
1999-09-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
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
190197
3012358417
3012358417
Lisa Ewing
1
N
2026-01-01
2875 Railroad St Pittsburgh PA US 15222