Hdc Corp.
United StatesFDA applicant, unverified
Hdc Corp. is a medical device manufacturer, with 62 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 62
Registry facts
- Registries
- FDA GUDID 32
- FDA 510(k) 30
- Device classes
- FDA Class II 58
- FDA Class I 2
What Hdc Corp. makes
Hdc Corp. manufactures orthodontic anchoring screws, reusable dental and maxillofacial surgical procedure kits that are non‑medicated, and reusable surgical screwdrivers, with the SPIDER SCREW being a representative device.
Catalogue
Search and filter all 62 devicesShowing 1-50 of 62
Frequently asked questions
How many devices does Hdc Corp. have in the registry?
The registry currently lists 62 devices for Hdc Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hdc Corp.'s devices?
Among its 50 most recently registered devices, Hdc Corp. has devices listed in FDA 510(k) (18 devices) and FDA GUDID (32 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Hdc Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Hdc Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hdc Corp. in the registry?
The most recently registered devices listed for Hdc Corp. include SPIDER SCREW SCL-1911, SPIDER SCREW SCL-1909, SPIDER SCREW SSM-1506 and SPIDER SCREW SCR-1907.