Daig Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 63
What Daig Corp. makes
Daig Corp. manufactures cardiac pacing components, including permanent and temporary pacemaker electrodes, lead introducers, and specialized catheters such as the Daig Pacel™ Flow Directed Pacing Catheter and Response™ Steerable Catheter. Their portfolio also includes adapters for pacemaker leads, unipolar lead configuration conductors, and modified labeling for lead introducers.
The company’s devices are regulated under FDA Class II and Class III classifications, with most submissions supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database. Daig Corp. is based in the United States.
Catalogue
Search and filter all 63 devicesShowing 1-50 of 63
Frequently asked questions
How many devices does Daig Corp. have in the registry?
The registry currently lists 63 devices for Daig Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Daig Corp.'s devices?
Among its 50 most recently registered devices, Daig Corp. has devices listed in FDA 510(k) (50 devices).
What risk classes do Daig Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Daig Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Daig Corp. in the registry?
The most recently registered devices listed for Daig Corp. include ADAPTER KIT, PACEMAKER, PERM. & TEMP., ELECTRODE, PERMANENT LEAD INTRADUCER and PACEMAKER, ELECTRODE.