Data / Medical devices / Canada / Kash Sales Inc.
Kash Sales Inc.: FDA-registered device maker in Richmond Hill Ontario, Canada, 39 510(k) clearances and 2 PMA approvals
Kash Sales Inc. is registered with the FDA (registration 3003120666) in Richmond Hill Ontario, Canada. It lists 48 device types. The FDA files 39 510(k) clearances and 2 PMA approvals under its listings, the newest dated May 9, 2023. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003120666
- Address
- 95 West Beaver Creek Road Unit 12, Richmond Hill Ontario, Canada, L4B 1H2
- Owner or operator
- Kash Sales Inc. (10062089)
- Roles
- Exporter to the US
- First device listed
- December 17, 2019
- Registered through
- 2027
- Brand names listed
- BEAUTIBOND, BEAUTIFIL II, BEAUTIFIL II LS, SURGICAL MASK
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 |
|---|---|---|---|---|---|---|
| May 9, 2023 | K212857 | Sterile Syringe for Single Use (with Needle), Sterile Hypodermic Needle for Single Use | FMF | Substantially Equivalent | Jiangsu Zhiyu Medical Instrument Co, Ltd. | accessdata.fda.gov |
| October 28, 2022 | K222581 | Stela Automix System | EBF | Substantially Equivalent | Sdi Limited | accessdata.fda.gov |
| August 30, 2022 | K214118 | Riva Cem Automix | EMA | Substantially Equivalent | Sdi Limited | accessdata.fda.gov |
| June 25, 2020 | K200175 | DIA-ROOT BIO Sealer | KIF | Substantially Equivalent | DiaDent Group International | accessdata.fda.gov |
| December 2, 2019 | K191656 | Zipbond | KLE | Substantially Equivalent | Sdi Limited | accessdata.fda.gov |
| January 2, 2019 | K183476 | 3M Filtek Universal Restorative | EBF | Substantially Equivalent | 3M Espe Dental Products | accessdata.fda.gov |
| September 6, 2016 | K160709 | HALYARD* PURPLE NITRILE XTRA* Powder-Free Exam Gloves | LZC | Substantially Equivalent | Halyard Health | accessdata.fda.gov |
| July 27, 2016 | K160596 | BEAUTIFIL II LS | EBF | Substantially Equivalent | Shofu Dental Corporation | accessdata.fda.gov |
| March 31, 2016 | K153708 | Halyard Black-Orange Powder-Free Nitrile Exam Glove | LZA | Substantially Equivalent | Halyard Health | accessdata.fda.gov |
| March 4, 2015 | K142990 | Insta-Gard Surgical and Procedure Face Mask | FXX | Substantially Equivalent | Cardinal Health200, LLC | accessdata.fda.gov |
| March 9, 2012 | K113423 | KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE | LZA | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| October 20, 2011 | K111402 | KC200, SURGICAL MASK, KC200, PROCEDURE MASK, KC300, SURGICALMASK, FLUIDSHIELD, KC300, PROCEDURE MASK, FLUIDSHIELD MODEL | FXX | Substantially Equivalent | Kimberly-Clark | accessdata.fda.gov |
| May 19, 2011 | K110302 | ADHESIVE EXL-759 | KLE | Substantially Equivalent | 3M Espe AG | accessdata.fda.gov |
| December 8, 2010 | K102984 | AURA | EBF | Substantially Equivalent | Sdi Limited | accessdata.fda.gov |
| August 23, 2010 | K101603 | BEAUTIFIL FLOW PLUS | EBF | Substantially Equivalent | Shofu Dental Corp. | accessdata.fda.gov |
| April 8, 2010 | K094007 | UNICEM | EMA | Substantially Equivalent | 3M Espe AG Dental Products | accessdata.fda.gov |
| December 11, 2008 | K082744 | BEAUTIBOND | KLE | Substantially Equivalent | Shofu Dental Corp. | accessdata.fda.gov |
| July 9, 2008 | K081260 | KIMBERLY-CLARK *LAVENDER* NITRILE POWER-FREE EXAM GLOVES | LZA | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| January 9, 2008 | K073296 | TEMPXN28 | EBG | Substantially Equivalent | 3M Espe AG Dental Products | accessdata.fda.gov |
| August 15, 2007 | K071742 | BEAUTIFIL II | EBF | Substantially Equivalent | Shofu Dental Corp. | accessdata.fda.gov |
| December 8, 2006 | K063237 | THERACAL LC | EJK | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| July 27, 2005 | K051867 | GRANDIO | EBF | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| April 7, 2004 | K040769 | STRUCTUR 2 SC | EBG | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| August 11, 2003 | K032001 | POLY Q (GARANT L, PENTA M, PENTA H) | ELW | Substantially Equivalent | 3M Espe AG Dental Products | accessdata.fda.gov |
| April 17, 2003 | K030516 | RIVA-SELF CURE | EMA | Substantially Equivalent | Southern Dental Industries, Inc. | accessdata.fda.gov |
| July 19, 2002 | K021475 | BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET | FMI | Substantially Equivalent | Bd | accessdata.fda.gov |
| October 22, 2001 | K012528 | ICE | EBF | Substantially Equivalent | Southern Dental Industries, Ltd. | accessdata.fda.gov |
| July 27, 2001 | K012060 | MODIFICATION TO:HU-FRIEDY BRAND SATIN SWIVEL ULTRASONIC INSERT | ELC | Substantially Equivalent | Hu-Friedy Mfg. Co., Inc. | accessdata.fda.gov |
| December 8, 1997 | K973091 | WAVE | EBF | Substantially Equivalent | Southern Dental Industries, Inc. | accessdata.fda.gov |
| March 1, 1995 | K945715 | MONOJECT(R) PISTON SYRINGES; 3,6,12,20,35 AND 60CC SIZES | FMF | Substantially Equivalent | Sherwood Medical Co. | accessdata.fda.gov |
| August 29, 1994 | K941991 | IN-ROOM AND SHARPSTAR | MMK | Substantially Equivalent | Sage Products, Inc. | accessdata.fda.gov |
| March 20, 1992 | K920424 | SCOTCHBOND BRAND MULTI-PURPOSE ADHESIVE SYSTEM | KLE | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| March 2, 1992 | K914476 | VITAPAN ACRYLIC DENTURE TEETH | ELM | Substantially Equivalent | Vident | accessdata.fda.gov |
| October 4, 1991 | K913537 | MEMOSIL C.D. | ELW | Substantially Equivalent | Heraeus Kulzer, Inc. | accessdata.fda.gov |
| August 11, 1988 | K882690 | IMPRINT VINYL POLYSILOXANE IMPRESSION MATERIAL | ELW | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| March 1, 1988 | K875133 | CAVIT-W | EBG | Substantially Equivalent | Espe GmbH (Us) | accessdata.fda.gov |
| July 23, 1985 | K852544 | MONOJECT STERILE 3CC SYRINGES W/ & WO/ NEEDLES | FMF | Substantially Equivalent | Sherwood Medical Co. | accessdata.fda.gov |
| August 31, 1978 | K781151 | REPROSIL | ELW | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
| February 28, 1978 | K780301 | CAULK TYLOK | EMA | Substantially Equivalent | L.D. Caulk Co. | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| September 30, 1999 | P990004 | SURGIFOAM ABSORBABLE GELATIN SPONGE, USP | LMF | 79 | September 18, 2026 | accessdata.fda.gov |
| October 14, 1960 | N12159 | SURGICEL BRAND ABSORBABLE HEMOSTAT | LMG | 120 | July 28, 2026 | accessdata.fda.gov |
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Updated September 18, 2026. 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.