HANURI DISTRIBUTION, INC

FDA Device Registration & Listing · Chatsworth, CA, US · Registration 3007778244

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007778244
FEI Number
3007778244
Entity Name
HANURI DISTRIBUTION, INC
City/State/Country
Chatsworth, CA, US
Establishment Address
9601 Owensmouth Ave Ste 8, Chatsworth, CA 91311, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hanuri distribution, inc (Owner Number: 10030065)
Owner / Operator Contact Address
9601 owensmouth ave. #8, Chatsworth, CA 91311, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K202044
PMA Number
N/A

All Registered Proprietary Names

Powerpress Cupping Set Powerpress Unit Powerpress Recovery Unit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNM Device, Pressure Applying Physical Medicine Class 1 890.5765 2012-07-13
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2011-12-08
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2011-12-08
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2020-11-09

Official Correspondent

jung moon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hanuri distribution, 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
K170216 Tactile Systems Technology, Inc. (Dba Tactile Medical) Flexitouch System 2017-05-26
K100306 Covidien KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES 2010-05-04
K242140 Jiale Health Technology Shenzhen Co., Ltd. Air Compression Leg Massager (K-705) 2025-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007778244. Last updated year: 2026. Please use registration number 3007778244 when referencing this establishment in official correspondence.
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