Data / Medical devices / Canada / Patterson Dental Canada Inc.
Patterson Dental Canada Inc.: FDA-registered device maker in Montreal Quebec, Canada, 18 510(k) clearances
Patterson Dental Canada Inc. is registered with the FDA (registration 3000219976) in Montreal Quebec, Canada. It lists 29 device types. The FDA files 18 510(k) clearances under its listings, the newest dated September 27, 2013. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3000219976
- Address
- 1205 henri Bourassa Blvd W., Montreal Quebec, Canada, H3M 3E6
- Owner or operator
- Patterson Companies, Inc. (9921026)
- Roles
- Exporter to the US, Foreign private label distributor, Repackager or relabeler
- First device listed
- August 25, 2005
- Registered through
- 2026
- Brand names listed
- 5-700;5-702;5801;5803;5804; CARB-EDGE; Carb-N-Sert; Integra; Jarit; Jarit Supercut; MicroFrance; Miltex; Padgett, ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION, AGENT, POLISHING, ABRASIVE, ORAL CAVITY, AGENT, TOOTH BONDING, RESIN, Bioactive Endosealer, CARB-EDGE; Carb-N-Sert; Jarit; Jarit Supercut; Miltex; Padgett, CARVER, WAX, DENTAL, CURETTE, OPERATIVE and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| September 27, 2013 | K130560 | MASTERTORQUE LUX 8900 L | EFB | Substantially Equivalent | Kaltenbach & Voigt GmbH | accessdata.fda.gov |
| May 11, 2011 | K110430 | DOLPHIN IMAGING | LLZ | Substantially Equivalent | Patterson Dental Supply, Inc. | accessdata.fda.gov |
| February 28, 2011 | K103399 | GENERAL DENISTRY MOTOR | EKX | Substantially Equivalent | Aseptico, Inc. | accessdata.fda.gov |
| July 22, 2009 | K091388 | GCUC-505 | EBF | Substantially Equivalent | GC America, Inc. | accessdata.fda.gov |
| February 15, 2008 | K080113 | APEX DAL ELECTRONIC APEX LOCATOR | LQY | Substantially Equivalent | Medicnrg , Ltd. | accessdata.fda.gov |
| May 31, 2007 | K070074 | LUBRINA, MODEL HIM-1 | EFB | Substantially Equivalent | J. Morita USA, Inc. | accessdata.fda.gov |
| October 19, 2006 | K062418 | K-SPRAY, MODEL 085-2715 | EFB | Substantially Equivalent | Scican | accessdata.fda.gov |
| October 2, 2006 | K062344 | GRANDIO SEAL | EBC | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| October 14, 2005 | K051705 | IPS E.MAX CAD/IPS E.MAX ZIRCAD | EIH | Substantially Equivalent | Ivoclar Vivadent, Inc. | accessdata.fda.gov |
| November 9, 2004 | K042819 | TETRIC EVOCERAM | EBF | Substantially Equivalent | Ivoclar Vivadent, Inc. | accessdata.fda.gov |
| March 15, 2004 | K040551 | COLTOLUX LED CURING LIGHT | EBZ | Substantially Equivalent | Coltene/Whaledent, Inc. | accessdata.fda.gov |
| January 23, 2004 | K033760 | ONE COAT SE BOND | KLE | Substantially Equivalent | Coltene/Whaledent, Inc. | accessdata.fda.gov |
| January 16, 2004 | K033585 | DIAPEX | KIF | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| February 7, 2002 | K013929 | HELIOMOLAR HB TRANSLUCENT SHADES | EBF | Substantially Equivalent | Ivoclar Vivadent, Inc. | accessdata.fda.gov |
| July 5, 2000 | K001518 | GRADIA | EBF | Substantially Equivalent | GC America, Inc. | accessdata.fda.gov |
| August 10, 1998 | K981663 | DIGITAL DOC | EIA | Substantially Equivalent | Digital Doc, LLC | accessdata.fda.gov |
| September 11, 1996 | K962543 | ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU | EFB | Substantially Equivalent | Nsk Nakanishi, Inc. | accessdata.fda.gov |
| September 29, 1995 | K942139 | SUPRASSON P MAX | ELC | Substantially Equivalent | Satelec | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Operative Dental, Accessories
- All makers of Carver, Wax, Dental
- All makers of Handpiece, Air-Powered, Dental
- All makers of Loupe, Binocular, Low Power
- All makers of Locator, Root Apex
- All makers of Forceps, Tooth Extractor, Surgical
Updated September 27, 2013. 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.