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CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Last updated May 24, 2026

What CLINICIAN'S CHOICE DENTAL PRODUCTS, INC. makes

The company manufactures a range of dental products, including rotary and reciprocating endodontic files, silicone dental impression materials, dental composite resins, and dental impression trays. They also produce diamond dental burs, endodontic paper points, and dental abrasive disks. Specific examples of their products include the Dual-Force Sectional Matrix System Wedge Kit, MPa Universal Light-Cure Universal Adhesive, and Typhoon Infinite Flex NiTi Files. The products are designed for various dental applications, such as impression taking, restorative procedures, and endodontic treatments. The company's portfolio includes both reusable and single-use devices.

The company's dental products are regulated as Class I, Class II, and U devices, and are listed in the FDA UDI registry. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of products does Clinician's Choice Dental Products, Inc. manufacture?

The company makes dental products, including endodontic files, impression materials, composite resins, and dental burs, for various dental applications.

Where is Clinician's Choice Dental Products, Inc. based?

The company is based in the United States.

Which registries list the company's devices?

The company's devices are listed in the FDA UDI registry.

How are the company's devices classified?

The devices are classified as Class I, Class II, or U devices, depending on their intended use and risk level.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: clinicianschoice.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)265-3444
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 626406016

Catalogue (1744)

Page 35 of 35

Device	Model / Reference	Registries	Class	Status
Affinity™ Multprep ® Wash w/o tips	632200W	FDA UDI	Class II	Active
CleanCut™ Extended Use Diamond FG 847KR-016C	1273196	FDA UDI	Class I	Active
Edge™ Diamond IOT016-4M Inlay/Onlay Taper	198643	FDA UDI	Class I	Unknown
D-Fine Double Diamond™ Primary Polisher Refill #09	131509	FDA UDI	Class I	Unknown
Edge™ Carbide Burs FG 7004 Round Gold Carbide Bur	3327004	FDA UDI	Class I	Unknown
True™ Dental Dam Latex 6x6	838236	FDA UDI	Class I	Active
Edge™ Diamond PC010-4.5C Parallel Chamfer	196044	FDA UDI	Class I	Unknown
Dr. Ronald Jordan Composite Instrument Series REJ #10	060110	FDA UDI	Class I	Active
Affinity™ Inflex FS Mega Mix 380ml	012385	FDA UDI	Class II	Active
Edge™ Diamond TMC014-6C Tapered Modified Chamfer	195464	FDA UDI	Class I	Unknown
EndoEssentials™ Absorbent Paper Points 100 - #40 .04 Taper	865440	FDA UDI	Class I	Active
Edge™ Diamond PS010-6.5M Parallel Shoulder	1961635	FDA UDI	Class I	Unknown
Edge™ Diamond ND010-4F Needle	191202	FDA UDI	Class I	Unknown
Edge™ Diamond PS111-014-8F Parallel Shoulder	1961125	FDA UDI	Class I	Unknown
Symmetry Facial Plane Relator Refill Kit	051048	FDA UDI	Class I	Active
X-Factor™ Minimally Invasive NiTi Files CM 30/.06 (25mm)	313603	FDA UDI	Class I	Active
Evanesce™ Nano-Enhanced Universal Restorative	320006	FDA UDI	Class II	Active
Edge™ Diamond ND016-5F Needle	191162	FDA UDI	Class I	Unknown
HeatWave™ Customizable Impression Trays Sizing Chart	188100	FDA UDI	Class I	Active
Edge™ Diamond FP016-4M (3.5) Football Pointed	192263	FDA UDI	Class I	Unknown
6.5 Mixing Tips "T-mixer"	033126	FDA UDI	Class I	Active
Edge™ Diamond ND008-3F Composite Needle	1912825	FDA UDI	Class I	Unknown
Clear Impression Trays Quadrant (Left)	036604	FDA UDI	Class I	Active
Evanesce™ Nano-Enhanced Universal Restorative Single Dose B1UX	323567	FDA UDI	Class II	Active
EndoEssentials™ Gutta Percha Points ISO#20 .02 Taper w MM Markings	861220	FDA UDI	Class I	Active
HeatWave™ Customizable Quadrant Impression Trays	188710	FDA UDI	Class I	Unknown
Convexi-T™ S2 Stainless Steel Convex Tofflemire™ Matrix Bands 6.3mm	206107	FDA UDI	Class I	Active
Typhoon™ Infinite Flex NiTi Files 20/.06 (21mm)	312161	FDA UDI	Class I	Active
Edge™ Diamond TS016-6M Tapered Shoulder	193163	FDA UDI	Class I	Active
Edge™ Diamond TC018-10.0M Tapered Chamfer	194813	FDA UDI	Class I	Unknown
Evanesce™ Nano-Enhanced Universal Restorative	320019	FDA UDI	Class II	Active
Edge™ Diamond PC016-8.5SC Parallel Chamfer	1960655	FDA UDI	Class I	Unknown
Edge™ Diamond ND018-10M Composite Needle	1912835	FDA UDI	Class I	Unknown
Edge™ Diamond R035-3.5EF Round	198351	FDA UDI	Class I	Unknown
Affinity™ Heavy Body Reg Set w/o tips 2pk	023400W	FDA UDI	Class II	Active
EndoEssentials™ Absorbent Paper Points 200 - F	866202	FDA UDI	Class I	Active
Edge™ Carbides FG701 Surgical Lenght Taper Xcut Carbide Bur	3357010	FDA UDI	Class I	Unknown
Typhoon™ Infinite Flex NiTi Files 20/.04 (21mm)	312141	FDA UDI	Class I	Active
X-Factor™ Minimally Invasive NiTi Files Assorted Sizes 25, 40, 60 (21mm)	311021	FDA UDI	Class I	Active
Edge™ Diamond ND012-6C Needle	191124	FDA UDI	Class I	Unknown
X-Factor™ Minimally Invasive NiTi Files 25/.03 (21mm)	311008	FDA UDI	Class I	Active
X-Factor™ Minimally Invasive NiTi Files 20/.04 (25mm)	311026	FDA UDI	Class I	Active
Template And Counter-Fit	K081017	FDA 510(k)	Class II	Active
Poly Siloxane Impression Material	K053014	FDA 510(k)	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

There is 1 recall record for Clinician's Choice Dental Products, Inc., initiated on March 18, 2022, with a status of terminated. The reason given for the recall is that the wrong compression material was packaged—specifically, Template Ultra Quick matrix material was included instead of the Heavy Body viscosity as indicated on the outer packaging of the 12PK.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Mar 18, 2022	Z-1100-2022	—	terminated	Wrong compression material - Template Ultra Quick matrix Material was packaged instead of the Heavy Body viscosity as indicated on the outer packaging of the 12PK