Crown Delta Corp.
United Statesfrom the FDA registration address FDA establishment FEI 2431069
Crown Delta Corp. is a medical device manufacturer, with 89 devices listed in FDA GUDID and FDA 510(k) (FDA Class II, Class I and Unclassified) as of 13 Nov 2026.
- Devices
- 89
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 71
- FDA 510(k) 18
- Device classes
- FDA Class II 64
- FDA Class I 24
- FDA Unclassified 1
- Identifiers
- FDA FEI 2431069
What Crown Delta Corp. makes
Crown Delta Corp. makes silicone dental impression materials, dental material mixing nozzles, and dental composite resins. Example products include Stabiliner, Impress-Rite, Perfecto, and Root Labs - VPS, along with various Impress-Rite mixing tips and ribbon tips.
The company's devices are classified as Class I, Class II, and unclassified (U) and are listed in the FDA 510(k) and FDA UDI registries.
Catalogue
Search and filter all 89 devicesShowing 1-50 of 89
Company details
- FDA FEI number
- 2431069
- Address
- 1520 FRONT ST., Yorktown, NY, 10598
Frequently asked questions
How many devices does CROWN DELTA CORP. have in the registry?
The registry currently lists 89 devices for CROWN DELTA CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CROWN DELTA CORP.'s devices?
Among its 50 most recently registered devices, CROWN DELTA CORP. has devices listed in FDA GUDID (50 devices).
What risk classes do CROWN DELTA CORP.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for CROWN DELTA CORP.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from CROWN DELTA CORP. in the registry?
The most recently registered devices listed for CROWN DELTA CORP. include Perecto DW64, STABILINER CD004, IMPRESS-RITE IMP-9009 and IMPRESS-RITE IMP-9008.