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CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

US

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
—
LinkedIn
—
Facebook
—
Phone
+1(800)265-3444
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
626406016

Catalogue (1744)

Page 3 of 35
DeviceModel / ReferenceRegistriesClassStatus
X-Factor™ Minimally Invasive NiTi Files 40/.03 (31mm) 311057
FDA UDI
Class IActive
Contours™ Finishing & Polishing Discs Refill Pack 3/8" Fine 133010
FDA UDI
Class IActive
Edge™ Diamond IC014M Inverted Cone 199643
FDA UDI
Class IUnknown
Edge™ Diamond PS014-8C Parallel Shoulder 1961445
FDA UDI
Class IUnknown
Edge™ Diamond IC016M Inverted Cone 199663
FDA UDI
Class IUnknown
Edge™ Diamond IOP010-4C Inlay/Onlay Parallel 199504
FDA UDI
Class IUnknown
Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 2 White 209002
FDA UDI
Class IActive
Counter-FIT™ Quick Mega Mix Cartridge 275380
FDA UDI
Class IIActive
Edge™ Diamond TS016-10SC Tapered Shoulder 193615
FDA UDI
Class IActive
Edge™ Diamond TC016-10F Tapered Chamfer 1946125
FDA UDI
Class IActive
Edge™ Diamond TS018-10M Tapered Shoulder 1938135
FDA UDI
Class IUnknown
Edge™ Diamond PMI016-5F Pear Minimally Invasive 1915625
FDA UDI
Class IUnknown
EndoEssentials™ Gutta Percha Points Size 35 .04 Taper w MM Markings 861435
FDA UDI
Class IActive
Edge™ Diamond PS014-6M Parallel Shoulder 1965635
FDA UDI
Class IUnknown
Edge™ Diamond TC012-8M Tapered Chamfer 1942835
FDA UDI
Class IActive
Edge™ Diamond PMI010-3M Pear Minimally Invasive 191313
FDA UDI
Class IUnknown
Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 3 Blue 209003
FDA UDI
Class IActive
Border-Lock® Green Mouldable Upper Dentulous Tray #47 187447
FDA UDI
Class IActive
Universal Precision Composite Instrument #5 (UPC5) 062115
FDA UDI
Class IUnknown
Edge™ Diamond FFE016-8M Flame Feather 197683
FDA UDI
Class IUnknown
Edge™ Diamond FR023-5.5M Football Round 1921335
FDA UDI
Class IUnknown
CleanCut™ Extended Use Diamond FG 856-025C| 1273220
FDA UDI
Class IActive
Edge™ Diamond TMC018-6M Tapered Modified Chamfer 195863
FDA UDI
Class IUnknown
Edge™ Diamond PS012-8M Parallel Shoulder 196123
FDA UDI
Class IUnknown
Affinity ™ Inflex FS 120ml Cartridge 012406
FDA UDI
Class IIActive
Evanesce™ Nano-Enhanced Universal Restorative 322514
FDA UDI
Class IIActive
Border-Lock® Green Mouldable Lower Dentulous Tray #58 187458
FDA UDI
Class IActive
Border-Lock® Autoclavable Lower Tray #52 185852
FDA UDI
Class IActive
Acu-Flow™ Putty Kit 1-016405
FDA UDI
Class IIUnknown
Edge™ Carbide Burs FG 7902 Needle Gold Carbide Bur 3327902
FDA UDI
Class IUnknown
Template® Clear 6pk 017916
FDA UDI
Class IIUnknown
Groovy Diamond® Polishing Brushes Mid-Size 6-Pack 650604
FDA UDI
Class IActive
Evanesce™ Nano-Enhanced Universal Restorative 322508
FDA UDI
Class IIActive
Inspire™ Esthetic Provisional Composite A1 152701
FDA UDI
Class IIActive
5.4 Dual-Port Mixing Tips (50-pack) 033523
FDA UDI
Class IActive
Border-Lock® Lower Tray #53 182153
FDA UDI
Class IActive
Dual-Force™ Sectional Matrix System Molar Rings Green 209008
FDA UDI
Class IActive
Groovy Diamond® Polishing Brushes Occlusal 6-Pack - No Jcard 655602
FDA UDI
Class IActive
Edge™ Carbide Burs KT1T Katana Carbide Bur 3331000
FDA UDI
Class IUnknown
Edge™ Carbide Burs FG 1156SS Operative Carbide Bur 3311561
FDA UDI
Class IUnknown
Edge™ Diamond TC018-11.5C Tapered Chamfer 1948145
FDA UDI
Class IUnknown
Acu-Flow™ Heavy Body 1-016402
FDA UDI
Class IIActive
Edge™ Diamond FP018.4.0F Football Pointed 1928425
FDA UDI
Class IUnknown
EdgeDam™ Refill Medium 6x6 Latex EDBLM6636
FDA UDI
Class IActive
Edge™ Diamond TS014-8C Tapered Shoulder 1934845
FDA UDI
Class IActive
Edge™ Carbide Burs FG 169L Taper Long Head Operative Carbide Bur 3311692
FDA UDI
Class IUnknown
Edge™ Carbide Burs FG 7642 Taper Round End Gold Carbide Bur 3327642
FDA UDI
Class IActive
EndoEssentials™ Absorbent Paper Points 100 - #35 .06 Taper 864635
FDA UDI
Class IActive
Edge™ Diamond PB012-8M Parallel Bevel 196283
FDA UDI
Class IUnknown
Edge™ Diamond TC012-10C Tapered Chamfer 1941245
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.

DateRecall No.ClassStatusReason
Mar 18, 2022Z-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