Data / Medical devices / United States / Jordco, Inc.
Jordco, Inc.: FDA-registered device maker in Hillsboro, OR, United States, 1 510(k) clearance
Jordco, Inc. is registered with the FDA (registration 3026760) in Hillsboro, OR, United States. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 14, 1999. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3026760
- FEI number
- 1000135335
- Address
- 8531 NE Cornell Rd. Ste 800, Hillsboro, OR, United States, 97124
- Owner or operator
- JORDCO, INC. (9006954)
- Roles
- Manufacturer
- First device listed
- May 12, 2001
- Registered through
- 2027
- Brand names listed
- ENDORING, Endogel, Endoring GelWell Cups: Accessory, Endoring High Density e-Foam Inserts: Accessory, Endoring II, Endoring Marking Tabs: Accessory, Endoring Metal Ruler: Accessory, Endoring Original and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Resin | KXR | 1 | Manufacturer | accessdata.fda.gov |
| Cleanser, Root Canal | KJJ | U | Manufacturer | accessdata.fda.gov |
| Disk, Abrasive | EHJ | 1 | Manufacturer | accessdata.fda.gov |
| File, Pulp Canal, Endodontic | EKS | 1 | Manufacturer | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Manufacturer | accessdata.fda.gov |
| Gauge, Depth, Instrument, Dental | EIL | 1 | Manufacturer | accessdata.fda.gov |
| Instruments, Dental Hand | DZN | 1 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 14, 1999 | K992484 | RCNG: ROOT CANAL NEGOTIATING GEL; MODEL RCNG | KJJ | Substantially Equivalent | Jordco, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Applicator, Resin
- All makers of Instruments, Dental Hand
- All makers of Disk, Abrasive
- All makers of Cleanser, Root Canal
- All makers of File, Pulp Canal, Endodontic
- All makers of Floss, Dental
Updated October 14, 1999. 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.