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Data / Medical devices / United States / JBC And Company

JBC And Company: FDA-registered device maker in Fredericksburg, TX, United States, 1 510(k) clearance

JBC And Company is registered with the FDA (registration 2954315) in Fredericksburg, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 24, 1998. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2954315
FEI number
3002768909
Address
10484 Ranch Road 965, Fredericksburg, TX, United States, 78624
Owner or operator
JBC AND COMPANY (9038527)
Roles
Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
July 21, 1999
Registered through
2026
Brand names listed
CO.'S ORTHODONTIC ACRYLIC RESINS, JBC'

Devices it lists

DeviceProduct codeClassRoleSource
Resin, Denture, Relining, Repairing, RebasingEBI2Manufacturer, Remanufacturer, Repackager 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
February 24, 1998K974727JET ACRYLIC LIQUID-MONOMER, ORTHO JET POWDER-POLYMER, PLASTICIZED METHACRYLATE HOMOPOLYMER, METHACRYLATE COPOLYMER, METREBISubstantially EquivalentJ.B.C and Co.accessdata.fda.gov

Compare with other makers

Updated February 24, 1998. 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.