JBC AND COMPANY

FDA Device Registration & Listing · Fredericksburg, TX, US · Registration 2954315

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2954315
FEI Number
3002768909
Entity Name
JBC AND COMPANY
City/State/Country
Fredericksburg, TX, US
Establishment Address
10484 Ranch Road 965, Fredericksburg, TX 78624, US
Establishment Type(s)
Remanufacture Medical Device,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
JBC AND COMPANY (Owner Number: 9038527)
Owner / Operator Contact Address
10484 Ranch Road 965, --, Fredericksburg, TX 78624, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K974727
PMA Number
N/A

All Registered Proprietary Names

JBC' CO.'S ORTHODONTIC ACRYLIC RESINS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 1999-07-21

Official Correspondent

PRISCILLA MIER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JBC AND COMPANY
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

Similar Registrations

Registration Number Establishment Name Location
3017374693 STRATASYS LTD - Headquarter Rehovot Central, IL
2950685 CO-ORAL-ITE DENTAL MFG. CO. DIAMOND SPRINGS, CA, US
3032727 TALON ACRYLICS, INC. Winchester, OR, US
3008320092 Shandong Huge Dental Material Corporation Rizhao Shandong, CN
1410097 GC AMERICA INC. ALSIP, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2954315. Last updated year: 2026. Please use registration number 2954315 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.