Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026760

FEI Number

1000135335

Entity Name

JORDCO, INC.

City/State/Country

Hillsboro, OR, US

Establishment Address

8531 NE Cornell Rd., Ste 800, Hillsboro, OR 97124, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

JORDCO, INC. (Owner Number: 9006954)

Owner / Operator Contact Address

8531 NE Cornell Rd., Ste 800, Hillsboro, OR 97124, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pure Bond Dispenser: Accessory to Resin Applicator e-Ruler Endogel Slickgel Pure Buff: Acrylic Polishing Wheels (refill pack) Pure Buff: Acrylic Polishing Kit Pure Floss Dispenser: Accessory to Floss Pure Floss Dispenser Cutter Cap Replacement : Accessory to Floss e-Dx Kit e-Dx Refill Pack Endoring Marking Tabs: Accessory ENDORING Endoring Metal Ruler: Accessory Endoring e-Foam Inserts: Accessory Endoring II Endoring High Density e-Foam Inserts: Accessory Endoring Original Endoring GelWell Cups: Accessory File Caddy Foam Inserts: Accessory to Endoring Files File Caddy: Accessory to Endoring Files

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXR	Applicator, Resin	Dental	Class 1	872.3140	2019-06-18
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2008-11-28
KJJ	Cleanser, Root Canal	Unknown	Class U	N/A	2007-11-15
EHJ	Disk, Abrasive	Dental	Class 1	872.6010	2001-05-12
JES	Floss, Dental	Dental	Class 1	872.6390	2019-06-18
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2008-11-28
EIL	Gauge, Depth, Instrument, Dental	Dental	Class 1	872.4565	2003-05-07
EKS	File, Pulp Canal, Endodontic	Dental	Class 1	872.4565	2019-06-18

Official Correspondent

JAMES JOHNSEN, D.M.D.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JORDCO, INC.

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
K882164	Arthur Blank & Co., Inc.	FLOSS CARD	1988-06-10
K864976	Endo Technic Corp.	SOLUSET CALCIUM DEMINERALIZING SOLUTION	1987-02-27

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0011-2020	Inter-Med Llc	U	Vista Dental Products CanalClean Endodontic Irrigation Kit, (1) 12mL - Chlor-XTRA, 6mL - SmearOFF + 92) + (2) 30ga Irrigation Tips + (1) Micro Aspirator with Tip, REF 504700
Z-0012-2020	Inter-Med Llc	U	Vista Dental Products Sodium Hypochlorite - 6%, 10 - 12cc Pre-filled Syringes, REF 502300
Z-0013-2020	Inter-Med Llc	U	Vista Dental Products Sodium Hypochlorite - 3%, 10 - 12cc Pre-filled Syringes, REF 502315
Z-0014-2020	Inter-Med Llc	U	Vista Dental Products Sodium Hypochlorite - 6%, QTY: 12, 3mL Pre-filled Syringes, REF 502350
Z-0015-2020	Inter-Med Llc	U	Vista Dental Products 3% Sodium Hypochlorite, 10- 3cc Pre-filled Syringes, REF 502355

Similar Registrations

Registration Number	Establishment Name	Location
3016447764	DSI DENTAL SOLUTIONS LTD	Ashdod Southern, IL
3010931810	CREDENTIS AG	Zug, CH
3015272949	Ormco Corporation	Brea, CA, US
3008370577	SHANGHAI SMEDENT MEDICAL INSTRUMENT CO., LTD	Shanghai, CN
3009420946	HUANGHUA PROMISEE DENTAL CO., LTD	Huanghua Hebei, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026760. Last updated year: 2026. Please use registration number 3026760 when referencing this establishment in official correspondence.