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Discus Dental, Inc.

US

Last updated September 17, 2026

Information

Country
US
Address
1700 A South Baker Ave, Ontario, CA, 91761
Website
—
LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
1000582314
DUNS Number
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Catalogue (39)

DeviceModel / ReferenceRegistriesClassStatus
Relief ACP DIS445/01
FDA UDI
Class IIActive
Philips Sonicare BreathRx DIS251/01
FDA UDI
Class IUnknown
Dash DIS429/01
FDA UDI
Class IUnknown
Philips Sonicare BreathRx DIS442/02
FDA UDI
Class IUnknown
Philips Zoom! Chairside Light-Activated Whitening Kit DIS556
FDA UDI
Class IIActive
Relief ACP DIS571/99
FDA UDI
Class IIActive
Philips Zoom! Chairside Light-Activated Whitening Kit DIS5714
FDA UDI
Class IIActive
Philips Zoom! WhiteSpeed IsoPrep Retractor DIS573
FDA UDI
Class IActive
Philips Sonicare BreathRx DIS359/11
FDA UDI
Class IUnknown
Philips Zoom! Protective Eyewear DIS203
FDA UDI
Class IActive
Philips Zoom! Relief ACP Oral Care Gel DIS455
FDA UDI
Class IIActive
Philips Zoom DIS578/01
FDA UDI
Class IActive
Philips Sonicare BreathRx DIS357/03
FDA UDI
Class IUnknown
Philips Relief ACP Oral Care Gel DIS272
FDA UDI
Class IIActive
Relief ACP DIS455/02
FDA UDI
Class IIActive
Philips Sonicare BreathRx DIS251/11
FDA UDI
Class IUnknown
Philips Zoom! IsoPrep Retractor DIS574
FDA UDI
Class IActive
Philips Zoom! WhiteSpeed Whitening LED Accelerator DIS558
FDA UDI
Class IActive
Philips Sonicare BreathRx DIS359/03
FDA UDI
Class IUnknown
Philips Zoom DIS716/01
FDA UDI
Class IUnknown
Philips Zoom! Chairside Light-Activated Whitening Kit DIS557
FDA UDI
Class IIActive
Philips Sonicare BreathRx DIS350/11
FDA UDI
Class IUnknown
Philips Sonicare BreathRx DIS442/01
FDA UDI
Class IUnknown
Philips Sonicare BreathRx DIS357/11
FDA UDI
Class IUnknown
Flash-Lite Ii Led Dental Curing Light K023748
FDA 510(k)
Class IIActive
Mega Bite Registration - Dental Bite Registration Material K030776
FDA 510(k)
Class IIActive
Simpliseal K093208
FDA 510(k)
Class IIActive
Dischem Chemical Proportioning & Dispensing System For Use With Cetylcide-G Concentrate And Diluent, Aquarius Model K033381
FDA 510(k)
Class IIActive
Sl3 K102639
FDA 510(k)
Class IIActive
Nuance K101215
FDA 510(k)
Class IIActive
Zen Cordless Prophy System K101612
FDA 510(k)
Class IActive
Flash-Lite Led Dental Curing Light K022184
FDA 510(k)
Class IIActive
Flashlite Rebel* K073518
FDA 510(k)
Class IIActive
Splash! Impression Material Device K052090
FDA 510(k)
Class IIActive
Precision Vps Impression Material K040053
FDA 510(k)
Class IIActive
Insight Ultrasonic Inserts K092417
FDA 510(k)
Class IIActive
Relief Acp Oral Care Gel K062176
FDA 510(k)
Class IIActive
Protege Ultrasonic Insert K051776
FDA 510(k)
Class IIActive
Proactive Care Prophylaxis Paste With Fluoride K033785
FDA 510(k)
Class IActive

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Oct 24, 2014Z-0425-2015—terminated

Product sold after April 1, 2014 were inadvertently filled with hydrogen peroxide teeth whitening gel (6% concentration as dispensed) on one side of the dual barrel syringe instead of the intended component (phosphate gel). Consequently, use of this product by patients may result in a neutral effect or increased sensitivity.

Jul 21, 2011Z-1186-2013—terminated

The firm is initiating this recall of the SL3 Soft Tissue Laser equipped with a fiber optic Unifiber system which contains a fragile glass filament because the fiber broke near the hand piece.