Manufacturer registered with FDA
J.B.C and Co.
Fredericksburg, TX, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 21998–2000
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 1990–2026
Devices listed with FDA
What J.B.C and Co. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Rebasing Repairing Relining Denture ResinEBI · Class 2 | Denture resins & teeth | Maker | CO.'S ORTHODONTIC ACRYLIC RESINSJBC' | 1999 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names J.B.C and Co. as the applicant.
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| JBC AND COMPANYFDA reg. 2954315 | Fredericksburg, TX, United States | Manufacturer, Remanufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9038527). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.