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Data / Medical devices / United States / Diamond Wipes International, Inc.

Diamond Wipes International, Inc.: FDA-registered device maker in Chino, CA, United States, 2 510(k) clearances

Diamond Wipes International, Inc. is registered with the FDA (registration 3003887639) in Chino, CA, United States. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 30, 2023. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3003887639
Address
4651 Schaefer Ave, Chino, CA, United States, 91710
Owner or operator
Diamond Wipes International, Inc. (10044119)
Roles
Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
May 1, 2013
Registered through
2026
Brand names listed
BioPlus+ No-Sting Barrier Film, CDx Diagnostics Slide Fixative, FreeDerm Adhesive Remover, Pap-Pack Cytology Fixative, TCS Concentrated Dental Appliance Cleaner, TCS Concentrated Denture Cleaner, after hours, date night and more

Devices it lists

DeviceProduct codeClassRoleSource
Cleanser, Denture, Over The CounterEFT1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Disinfectant, Medical DevicesLRJ1Contract manufactureraccessdata.fda.gov
Fixative, Alcohol ContainingLDZ1Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Lubricant, PersonalNUC2Repackager or relabeleraccessdata.fda.gov
Solvent, Adhesive TapeKOX1Contract manufactureraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Contract manufactureraccessdata.fda.gov

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 30, 2023K222567Playground For All Love SeshNUCSubstantially EquivalentPlayground For Allaccessdata.fda.gov
May 23, 2008K080631CLEANSE.FRESHEN.GO; ALIGNER CLEANSING TOWELETTE AND DENTAL APPLIANCE CLEANSEREFTSubstantially EquivalentOral Health Technologies, LLCaccessdata.fda.gov

Compare with other makers

Updated January 30, 2023. 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.