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Data / Medical devices / United States / Precision Fabrics Group, Inc.

Precision Fabrics Group, Inc.: FDA-registered device maker in Greensboro, NC, United States, 1 510(k) clearance

Precision Fabrics Group, Inc. is registered with the FDA (registration 1066748) in Greensboro, NC, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 25, 2007. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1066748
FEI number
1000230631
Address
301 East Meadowview Road, Greensboro, NC, United States, 27406
Owner or operator
Precision Fabrics Group Inc. (10025527)
Roles
Manufacturer, Specification developer
First device listed
April 21, 2008
Registered through
2026
Brand names listed
DermaTherapy Fabrics, Essentia, Pristine

Devices it lists

DeviceProduct codeClassRoleSource
Cover, Mattress (Medical Purposes)FMW1Manufactureraccessdata.fda.gov
Fiber, Medical, AbsorbentFRL1Manufacturer, Specification developeraccessdata.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 25, 2007K061242DERMATHERAPY, MODEL 22216FMWSubstantially EquivalentPrecision Fabrics Group, Inc.accessdata.fda.gov

Compare with other makers

Updated January 25, 2007. 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.