Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1450371

FEI Number

1450371

Entity Name

MEDI USA, LP

City/State/Country

WHITSETT, NC, US

Establishment Address

6481 Franz Warner Pkwy, WHITSETT, NC 27377, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

MEDI USA, LP (Owner Number: 1450371)

Owner / Operator Contact Address

6481 FRANZ WARNER PKWY., Whitsett, NC 27377, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

medi pneumatic compression system (pcs) - brio (Model 651) medi pneumatic compression system (pcs) - genius (Model 652) circaid juxtalite circaid reduction kit circaid juxtafit circaid juxtacures (compression ulcer recovery systems) circaid graduate circaid power added compression (pac) band circaid customizable hand wrap circaid customizable interlocking ankle foot wrap circaid single band ankle foot wrap (afw) restiffic relief circaid juxtalite HD circaid reduction kit head & neck Norton Hand Solution circaid reduction kit vest Doc Ortho relief circaid compression anklet Compressive Undersock Duomed Relax Mediven Active Cotton Mediven Comfort Sculpt Leggings Rejuva Duomed Advantage Brace Liner Duomed Soft Stripe Restiffic RLS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JOW	Sleeve, Limb, Compressible	Cardiovascular	Class 2	870.5800	2019-06-17
JOW	Sleeve, Limb, Compressible	Cardiovascular	Class 2	870.5800	2022-09-20
MDR	Binder, Medical, Therapeutic	General Hospital	Class 1	880.5160	2016-12-22
FQL	Stocking, Medical Support (For General Medical Purposes)	General Hospital	Class 1	880.5780	2016-12-22
DWL	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)	General Hospital	Class 2	880.5780	2018-07-19
OTX	Foot Wrap For Treating Restless Leg Syndrome Symptoms	Physical Medicine	Class 1	890.5760	2017-08-15

Official Correspondent

John Cody

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDI USA, LP

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

Similar Registrations

Registration Number	Establishment Name	Location
3033981998	KOYA MEDICAL, INC.	Dallas, TX, US
3020703724	Therma Bright Inc.	Toronto Ontario, CA
3014491159	AIROS MEDICAL INC	Audubon, PA, US
3014834638	ZENITH TECHNICAL INNOVATIONS, LLC	Gurnee, IL, US
3009155917	GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1450371. Last updated year: 2026. Please use registration number 1450371 when referencing this establishment in official correspondence.