FEI 1000306694
Tecomet, Inc.
5307 95th Ave, KENOSHA, WI, US
MDR events8All time
Recalls0All time
Registered products62
Establishment typeRepackRepack or Relabel Medical Device
Registered product codes
62 product codes
Recent MDR events
8 on file
- TORQUE LIMITING DRIVER HANDLENov 17, 2023Injury1000306694-2023-00001
- TECOMETApr 2, 2021Malfunction11607199
- TECOMETMar 23, 2021Malfunction11552963
- CONCEPT LINEAR WIDE BITE PUNCH, STRAIGHTNov 14, 2019Malfunction1017294-2019-00147
- CONCEPT LINEAR WIDE BITE PUNCH, STRAIGHTJun 13, 2019Malfunction1017294-2019-00069
- CONCEPT LINEAR WIDE BITE PUNCH, STRAIGHTMay 30, 2019Malfunction1017294-2019-00065
- CONCEPT LINEAR WIDE BITE PUNCH, STRAIGHTJul 2, 2018Malfunction1017294-2018-00101
- CONCEPT LINEAR WIDE BITE PUNCH, UP 15 DEGREEMay 10, 2018Injury1017294-2018-00063
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 1000306694.
FDA inspections
2 on file
- No Action Indicated (NAI)Feb 19, 2026
Compliance: Devices
- No Action Indicated (NAI)Feb 19, 2026
Postmarket Assurance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.