Intermedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 211
What Intermedics, Inc. makes
Intermedics, Inc. manufactures cardiac pacing components, including unipolar and bipolar pacing leads (e.g., Model 480-01, Poly Flex implantable pacing lead), implantable pulse generators, lead adapters (e.g., GE Lead Adapter Model 345-01, Adaptaid Lead Adapter #365-17), and header plugs (e.g., Model 366-15 VS 1). The company also produces tools like a syringe driver (MS-16) and a lensometer (Veri-Vu), as well as splicing crimps and sleeves for implant aids. Their product line covers both external and implanted cardiac devices, with a focus on pacing systems and related accessories.
The company’s devices are classified under FDA categories Class I, Class II, and Class III, with submissions recorded in the FDA 510(k) registry. These products are listed under U.S. regulatory oversight, and the company is headquartered in the United States.
Catalogue
Search and filter all 211 devicesShowing 1-50 of 211
Frequently asked questions
How many devices does Intermedics, Inc. have in the registry?
The registry currently lists 211 devices for Intermedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intermedics, Inc.'s devices?
Among its 50 most recently registered devices, Intermedics, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Intermedics, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Intermedics, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Intermedics, Inc. in the registry?
The most recently registered devices listed for Intermedics, Inc. include LIFELINE -UNIPOLAR LEAD #487-05, IMPLANT AID SPLICING CRIMP & SLEEVE, VERI-VU LENSOMETER and IMPLANTABLE PULSE GENERATOR PACEMAKERS.