Tpl-Cordis, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Tpl-Cordis, Inc. makes
Tpl-Cordis, Inc. manufactures cardiac pacemakers, including the Model 255A Programmer III with software revisions, the Vicor Pacer (Model 410A), and modified versions of the Multicor, Ancór, and Omni-Stanicór pacemakers. Their portfolio also includes modified Ancór and Hi-Flex unipolar active fixation leads for pacemaker systems.
These devices fall under Class III regulatory classification in the U.S. and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Model 255A Programmer Iii, W/Software Revi. 4004 Ref K882429
Regimes: 510(k) Registry: 510(k)Vicor Pacer, Model 410A Ref K880432
Regimes: 510(k) Registry: 510(k)Vicor, Model 410A Ref K873202
Regimes: 510(k) Registry: 510(k)Modified Multicor And Omni-Stanicor Pacemakers Ref K873158
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Multicor And Pacemakers Ref K880898
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tpl-Cordis, Inc. have in the registry?
The registry currently lists 6 devices for Tpl-Cordis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tpl-Cordis, Inc.'s devices?
Among its 6 most recently registered devices, Tpl-Cordis, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Tpl-Cordis, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Tpl-Cordis, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Tpl-Cordis, Inc. in the registry?
The most recently registered devices listed for Tpl-Cordis, Inc. include MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004, VICOR PACER, MODEL 410A, VICOR, MODEL 410A and MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERS.