Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019130

FEI Number

3019130

Entity Name

D. E. HOKANSON, INC.

City/State/Country

BELLEVUE, WA, US

Establishment Address

12840 NE 21ST PL, BELLEVUE, WA 98005, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

D. E. HOKANSON, INC. (Owner Number: 3019130)

Owner / Operator Contact Address

12840 N.E. 21ST PL., --, Bellevue, WA 98005, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K932851

PMA Number

N/A

All Registered Proprietary Names

TD-312 CALCULATING CUFF INFLATOR UDC1.9 Durable Digit Cuff UPC3.3 Durable Digit or Penile Cuff UPC2.5 Durable Digit or Penile Cuff UDC1.6 Durable Digit Cuff UDC2.5 Durable Digit Cuff AG101 AIR SOURCE FOR E20 E-20 RAPID CUFF INFLATOR EC-6 PLETHYSMOGRAPH AI6 Arterial Inflow System MD6 Doppler and MD6VR Chart Recorder MD 35 PROCORD SYSTEM DP2 Disposable Digit or Penile Cuff DP2.5 Disposable Digit or Penile Cuff

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXN	System, Measurement, Blood-Pressure, Non-Invasive	Cardiovascular	Class 2	870.1130	1992-06-30
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	1992-06-30
DXN	System, Measurement, Blood-Pressure, Non-Invasive	Cardiovascular	Class 2	870.1130	1992-06-30
JOM	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	Cardiovascular	Class 2	870.2780	2006-06-07
JOM	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	Cardiovascular	Class 2	870.2780	2007-12-11
DXK	Echocardiograph	Cardiovascular	Class 2	870.2330	2006-06-07
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2006-06-07
DXN	System, Measurement, Blood-Pressure, Non-Invasive	Cardiovascular	Class 2	870.1130	2006-06-07
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2006-06-07

Official Correspondent

KYRA GRAY

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

D. E. HOKANSON, 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
K100940	Andon Health Co, Ltd.	FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965	2010-06-29
K251581	Shenzhen Hingmed Medical Instrument Co., Ltd.	Wearable Ambulatory Blood Pressure Monitor (WBP-02A)	2026-02-13
K200521	Health & Life Co., Ltd.	Full Automatic(NIBP) Blood Pressure Monitor	2020-06-12
K152003	Andon Health Co, Ltd.	iHealth BP3L Wireless Blood Pressure Monitor	2015-09-24
K952827	Sein Electronics Co., Ltd.	FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000	1996-11-14

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0032-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.

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3011912849	BODYTRACE	San Jose, CA, US
3036999955	ZYBS CONSULTING LLC DBA ZYBS MEDICAL GROUP, DBA ZYBS MEDICAL	Largo, MD, US
3019575688	AKTIIA SA	Neuchatel, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019130. Last updated year: 2026. Please use registration number 3019130 when referencing this establishment in official correspondence.