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Data / Medical devices / United States / Virginia Industries For The Blind

Virginia Industries For The Blind: FDA-registered device maker in Richmond, VA, United States, 5 510(k) clearances

Virginia Industries For The Blind is registered with the FDA (registration 1119294) in Richmond, VA, United States. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated April 21, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1119294
Address
1535 High St, Richmond, VA, United States, 23220
Owner or operator
VA DEPT. FOR THE BLIND AND VISION IMPAIRED (9001609)
Roles
Repackager or relabeler
First device listed
December 18, 2013
Registered through
2026
Brand names listed
Soft Touch

Devices it lists

DeviceProduct codeClassRoleSource
Latex Patient Examination GloveLYY1Repackager or relabeleraccessdata.fda.gov
Medical Glove, SpecialtyLZC1Repackager or relabeleraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Repackager or relabeleraccessdata.fda.gov
Vinyl Patient Examination GloveLYZ1Repackager or relabeleraccessdata.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
April 21, 2016K152222NITRILE BLUE POWDER FREE EXAMINATION GLOVES tested for use with Chemotheraphy DrugsLZCSubstantially EquivalentGmp Medicare Sdn Bhd (F25)accessdata.fda.gov
February 5, 2015K141982DERMAGRIP POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVES, NON-STERILE, TESTED FOR USE WITH CHEMOTHERAPY DRUGSLZCSubstantially EquivalentWrp Asia Pacific Sdn. Bhd.accessdata.fda.gov
November 4, 2011K111923SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILELYYSubstantially EquivalentPt. Intan Hevea Industryaccessdata.fda.gov
March 20, 2007K063627POWDER FREE NITRILE EXAMINATION GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUGS (BLUE)LZASubstantially EquivalentSmart Glove Corp. Sdn Bhdaccessdata.fda.gov
June 21, 2005K051148POWDER-FREE VINYL PATIENT EXAMINATION GLOVESLYZSubstantially EquivalentZibo Sinocare Plastic Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 21, 2016. 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.