Oscor Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 31
What Oscor Medical Corp. makes
Oscor Medical Corp. manufactures implantable and temporary pacing leads, including unipolar and bipolar designs, as well as retractable and tined modifications for cardiac pacing applications. Their portfolio also includes specialized tools like a pacer sensing analyzer and a disposable catheter for stone extraction. Hemostasis valves, with or without side ports, are part of their product line for procedural use.
The company’s devices are classified under FDA Class II and Class III, with regulatory submissions recorded in the FDA 510(k) database. Their products are listed in the US under the jurisdiction of the Food and Drug Administration. The manufacturer is based in the United States.
Catalogue
Search and filter all 31 devicesFrequently asked questions
How many devices does Oscor Medical Corp. have in the registry?
The registry currently lists 31 devices for Oscor Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oscor Medical Corp.'s devices?
Among its 31 most recently registered devices, Oscor Medical Corp. has devices listed in FDA 510(k) (31 devices).
What risk classes do Oscor Medical Corp.'s devices fall under?
Among its 31 most recently registered devices, the classes recorded for Oscor Medical Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Oscor Medical Corp. in the registry?
The most recently registered devices listed for Oscor Medical Corp. include IMPLANT PACING LEAD TINED #3390, MODIFICATION, MISCELLANEOUS PACING LEAD, PACER SENSING ANALYZER (PSA 100) and PRODUCTS IMPLANT PACING LEAD, TINED, MODIFICATION.