Data / Medical devices / United States / Creodent Hudson Valley

Creodent Hudson Valley: FDA-registered device maker in Fishkill, NY, United States, 10 510(k) clearances

Name: Creodent Hudson Valley FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Creodent Hudson Valley is registered with the FDA (registration 3030255892) in Fishkill, NY, United States. It lists 4 device types. The FDA files 10 510(k) clearances under its listings, the newest dated February 10, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3030255892
Address: 1769 Rt 52, Fishkill, NY, United States, 12524
Owner or operator: Creodent Hudson Valley (10089653)
Roles: Manufacturer
First device listed: December 26, 2023
Registered through: 2026
Brand names listed: CreoKorrekt Aligners, CreoZ, Solidex

Devices it lists

Device	Product code	Class	Role	Source
Abutment, Implant, Dental, Endosseous	NHA	2	Manufacturer	accessdata.fda.gov
Aligner, Sequential	NXC	2	Manufacturer	accessdata.fda.gov
Crown, Preformed	ELZ	1	Manufacturer	accessdata.fda.gov
Dental Abutment Design Software For Dental Laboratory	PNP	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
February 10, 2026	K251515	Solidex® Ti-Links and Screws	NHA	Substantially Equivalent	CreoDent Hudson Valley	accessdata.fda.gov
December 2, 2022	K220390	CreoDent Solidex Customized Abutment and Screw	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
October 13, 2022	K211427	CREOKORREKT Aligners	NXC	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
April 2, 2021	K202909	CreoDent Solidex Customized Abutment	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
December 16, 2020	K202095	CreoDent Solidex Customized Abutment and Screw	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
July 18, 2017	K170100	CreoDent Solidex Customized Abutment and Screw	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
May 8, 2017	K162734	CreoDent Solidex Customized Abutment	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
September 29, 2016	K160436	CreoDent Solidex Custom Abutment	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
June 4, 2015	K150012	CreoDent Solidex Customized Abutment	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov
September 17, 2013	K113738	CREODENT SOLIDEX CUSTOM ABUTMENT	NHA	Substantially Equivalent	Creodent Prosthetics, Ltd.	accessdata.fda.gov

Compare with other makers

Updated February 10, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.