Denq
South KoreaFDA applicant, unverified
Denq is a medical device manufacturer, with 668 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 668
Registry facts
- Registries
- FDA GUDID 667
- FDA 510(k) 1
- Device classes
- FDA Class II 666
- FDA Class I 2
What Denq makes
Denq manufactures two-piece basket endosteal dental implants designed for subperiosteal placement, including fixtures with SLA (Sandblasted, Large-grit, Acid-etched) surface treatments. These devices are intended for dental applications requiring osseointegration with bone, such as partial or full arch reconstructions.
The company’s portfolio is regulated under FDA Class II devices, with products listed via 510(k) premarket notifications and the FDA’s Unique Device Identifier (UDI) system. These devices are intended for use in the United States.
Catalogue
Search and filter all 668 devicesShowing 1-50 of 668
Frequently asked questions
How many devices does Denq have in the registry?
The registry currently lists 668 devices for Denq. Devices recorded under merged duplicate company entries are counted once.
Which registries list Denq's devices?
Among its 50 most recently registered devices, Denq has devices listed in FDA GUDID (50 devices).
What risk classes do Denq's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Denq's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Denq in the registry?
The most recently registered devices listed for Denq include DenQ Sub SLA Fixture I DSSR35070S, DenQ Sub SLA Fixture I DSSR35075S, DenQ Sub SLA Fixture I DSSR35080S and DenQ Sub SLA Fixture I DSSR35085S.