Registered with FDA
Kash Sales Inc.
Richmond Hill, Canada. Lists 38 dental device types with FDA across 1 registered establishment.
- Device types listed
- 38
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Canada
Devices listed with FDA
What Kash Sales Inc. currently lists, by FDA device type, with the brand and model names on the listing.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Kash Sales Inc. lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Sdi Limited (4), Shofu Inc (4), 3M Espe AG Dental Products (3), Southern Dental Industries, Inc. (3), Voco GmbH (2), 3M Company (2), DiaDent Group International (1), 3M Espe Dental Products (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 28 Oct 2022 | K222581 | Stela Automix System | Sdi Limited | EBF Resin Tooth Shade Material |
| 30 Aug 2022 | K214118 | Riva Cem Automix | Sdi Limited | EMA Dental Cement |
| 25 Jun 2020 | K200175 | DIA-ROOT BIO Sealer | DiaDent Group International | KIF Root Canal Filling Resin |
| 2 Dec 2019 | K191656 | Zipbond | Sdi Limited | KLE Resin Tooth Bonding Agent |
| 2 Jan 2019 | K183476 | 3M Filtek Universal Restorative | 3M Espe Dental Products | EBF Resin Tooth Shade Material |
| 27 Jul 2016 | K160596 | BEAUTIFIL II LS | Shofu Inc | EBF Resin Tooth Shade Material |
| 19 May 2011 | K110302 | ADHESIVE EXL-759 | 3M Espe AG | KLE Resin Tooth Bonding Agent |
| 8 Dec 2010 | K102984 | AURA | Sdi Limited | EBF Resin Tooth Shade Material |
| 23 Aug 2010 | K101603 | BEAUTIFIL FLOW PLUS | Shofu Inc | EBF Resin Tooth Shade Material |
| 8 Apr 2010 | K094007 | UNICEM | 3M Espe AG Dental Products | EMA Dental Cement |
| 11 Dec 2008 | K082744 | BEAUTIBOND | Shofu Inc | KLE Resin Tooth Bonding Agent |
| 9 Jan 2008 | K073296 | TEMPXN28 | 3M Espe AG Dental Products | EBG Resin Temporary Crown and Bridge |
| 15 Aug 2007 | K071742 | BEAUTIFIL II | Shofu Inc | EBF Resin Tooth Shade Material |
| 8 Dec 2006 | K063237 | THERACAL LC | Bisco, Inc. | EJK Calcium Hydroxide Cavity Liner |
| 27 Jul 2005 | K051867 | GRANDIO | Voco GmbH | EBF Resin Tooth Shade Material |
| 7 Apr 2004 | K040769 | STRUCTUR 2 SC | Voco GmbH | EBG Resin Temporary Crown and Bridge |
| 11 Aug 2003 | K032001 | POLY Q (GARANT L, PENTA M, PENTA H) | 3M Espe AG Dental Products | ELW Impression Material |
| 17 Apr 2003 | K030516 | RIVA-SELF CURE | Southern Dental Industries, Inc. | EMA Dental Cement |
| 22 Oct 2001 | K012528 | ICE | Southern Dental Industries, Inc. | EBF Resin Tooth Shade Material |
| 27 Jul 2001 | K012060 | MODIFICATION TO:HU-FRIEDY BRAND SATIN SWIVEL ULTRASONIC INSERT | Hu-Friedy Mfg Co., LLC | ELC Ultrasonic Scaler |
| 8 Dec 1997 | K973091 | WAVE | Southern Dental Industries, Inc. | EBF Resin Tooth Shade Material |
| 20 Mar 1992 | K920424 | SCOTCHBOND BRAND MULTI-PURPOSE ADHESIVE SYSTEM | 3M Company | KLE Resin Tooth Bonding Agent |
| 2 Mar 1992 | K914476 | VITAPAN ACRYLIC DENTURE TEETH | Vident | ELM Teeth Plastic Denture |
| 4 Oct 1991 | K913537 | MEMOSIL C.D. | Heraeus Kulzer, LLC | ELW Impression Material |
| 11 Aug 1988 | K882690 | IMPRINT VINYL POLYSILOXANE IMPRESSION MATERIAL | 3M Company | ELW Impression Material |
| 1 Mar 1988 | K875133 | CAVIT-W | Espe GmbH (Us) | EBG Resin Temporary Crown and Bridge |
| 31 Aug 1978 | K781151 | REPROSIL | Dentsply Intl., Inc. | ELW Impression Material |
| 28 Feb 1978 | K780301 | CAULK TYLOK | L.D. Caulk Co. | EMA Dental Cement |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| KASH SALES INC.FDA reg. 3003120666 | Richmond Hill Ontario, Canada | Foreign exporter |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10062089). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.