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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 2 of 35
DeviceModel / ReferenceRegistriesClassStatus
EndoEssentials™ Gutta Percha Points ISO#70 .02 Taper w MM Markings 861270
FDA UDI
Class IActive
Edge™ Carbide Burs FG 556 Flat Fissure Xcut Operative Carbide Bur 3315560
FDA UDI
Class IUnknown
EndoEssentials™ Absorbent Paper Points 200 - ISO#35-.02 Taper 864235
FDA UDI
Class IActive
Edge™ Diamond TS016-6C Tapered Shoulder 1931645
FDA UDI
Class IActive
Evanesce™ Nano-Enhanced Universal Restorative 322529
FDA UDI
Class IIActive
EndoEssentials™ Absorbent Paper Points 200 - ISO#30-.02 Taper 864230
FDA UDI
Class IActive
Edge™ Diamond FR023-5.5M Football Round 192133
FDA UDI
Class IUnknown
Yellow Intraoral Tips 032520
FDA UDI
Class IActive
Quad-Tray® Xtra Long XL 041400
FDA UDI
Class IActive
X-Factor™ Minimally Invasive NiTi Files 25/.03 (31mm) 311052
FDA UDI
Class IActive
Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 1 Purple 209001
FDA UDI
Class IActive
Edge™ Diamond TMC016-10C Tapered Modified Chamfer 1956145
FDA UDI
Class IUnknown
X-Factor™ Minimally Invasive NiTi Files 60/.02 (25mm) 311039
FDA UDI
Class IActive
Edge™ Diamond R012-1.1M Round 1981235
FDA UDI
Class IUnknown
EndoEssentials™ Gutta Percha Points F2 - EE PT Series 863602
FDA UDI
Class IActive
EndoEssentials™ Gutta Percha Points FF - Non-Standard Accessory 862101
FDA UDI
Class IActive
Edge™ Diamond PC014-6.5C Parallel Chamfer 196464
FDA UDI
Class IUnknown
Edge™ Carbide Burs FG 558 Flat Fissure Xcut Operative Carbide Bur 3315580
FDA UDI
Class IUnknown
Acu-Flow™ Heavy Body 1-016407
FDA UDI
Class IIUnknown
Border-Lock® Green Mouldable Lower Dentulous Tray #57 187457
FDA UDI
Class IActive
Contours™ Finishing & Polishing Discs 3/8" Starter Kit 133002
FDA UDI
Class IActive
Edge™ Carbide Burs EF4 Gold Carbide Bur 3324100
FDA UDI
Class IUnknown
Large (White) Intraoral Tips 032110
FDA UDI
Class IActive
Green Mouldable Edentulous Trays Size 23 188423
FDA UDI
Class IUnknown
Evanesce™ flow flowable restorative A1E 323501
FDA UDI
Class IIActive
EndoEssentials™ Absorbent Paper Points 100 - F3 EEPT Series 866103
FDA UDI
Class IActive
Evanesce™ flow flowable restorative single dose BL1U 323555
FDA UDI
Class IIUnknown
BULK Affinity™ Inflex FS Mega Mix 012306
FDA UDI
Class IIActive
Edge™ Diamond TC012-6SC Tapered Chamfer 194265
FDA UDI
Class IActive
Edge™ Diamond TC016-10M Tapered Chamfer 194613
FDA UDI
Class IActive
Convexi-T™ Convex Toflemire™ Matrix Bands 5.5mm 206106
FDA UDI
Class IActive
7.5 Mixing Tips 033124
FDA UDI
Class IActive
Groovy Diamond® Polishing Brushes Universal Sample Pack 976501
FDA UDI
Class IActive
Affinity™ Spectrum Quick Bite 18pk 016918
FDA UDI
Class IIUnknown
Edge™ Carbide Burs OF 1 Gold Carbide Bur 3321000
FDA UDI
Class IUnknown
Template® Ultra Quick Matrix Material 36pk 018936
FDA UDI
Class IIActive
Border-Lock® Autoclavable Upper Tray #47 185847
FDA UDI
Class IActive
Edge™ Diamond IOT025-4M Inlay/Onlay Taper 1982535
FDA UDI
Class IUnknown
Edge™ Diamond TC025-8C Tapered Chamfer 194584
FDA UDI
Class IActive
Edge™ Diamond TS012-6SC Tapered Shoulder 193125
FDA UDI
Class IUnknown
Re-Cord™ Knitted Retraction Cord #1 649104
FDA UDI
UActive
EndoEssentials™ Gutta Percha Points MF - Non-Standard Accessory 862102
FDA UDI
Class IActive
Edge™ Diamond FP016-4M (3.5) Football Pointed 1922635
FDA UDI
Class IUnknown
Edge™ Diamond TC012-8C Tapered Chamfer 1942845
FDA UDI
Class IActive
X-Factor™ Minimally Invasive NiTi Files 40/.01 (31mm) 311055
FDA UDI
Class IActive
EndoEssentials™ Absorbent Paper Points 100 - #20 .06 Taper 864620
FDA UDI
Class IActive
Acu-Flow™ Medium Body 1-016408
FDA UDI
Class IIActive
Border-Lock® Green Mouldable Upper Dentulous Tray 187401
FDA UDI
Class IActive
Evanesce™ Nano-Enhanced Universal Restorative 320009
FDA UDI
Class IIActive
5.4 Dual-Port Mixing Tips (12 pack) 970305
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