Data / Medical devices / Crown And Bridge, Temporary, Resin / Japan
FDA-registered makers of Crown And Bridge, Temporary, Resin in Japan: 6 establishments
6 establishments in Japan are registered with the FDA to make Crown And Bridge, Temporary, Resin (product code EBG). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Crown And Bridge, Temporary, Resin
- Product code
- EBG
- Country
- Japan
Makers of Crown And Bridge, Temporary, Resin in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| GC Dental Products Corp. | KASUGAI-SHI Aichi, Japan | Manufacturer | 4 | September 5, 2014 | 0 | 0 | 0 | api.fda.gov |
| GC Corp. | ITABASHI-KU Tokyo, Japan | Complaint file establishment, Exporter to the US, Manufacturer | 2 | January 16, 2001 | 0 | 0 | 0 | api.fda.gov |
| Neo Dental Chemical Products Co., Ltd. | Nagano, Japan | Manufacturer | 1 | September 7, 2011 | 0 | 0 | 0 | api.fda.gov |
| Yamahachi Dental MFG. Co. | Gamagori City Aichi, Japan | Complaint file establishment, Specification developer | 1 | November 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Shiga Shofu Inc. | Koka Shiga, Japan | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shofu Inc. | FUKUINE, HIGASHIYAMA-KU Kyoto, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.