Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1450790

FEI Number

1450790

Entity Name

JW NORTH AMERICA, INC.

City/State/Country

Rockland, MA, US

Establishment Address

200 Ledgewood Place, Suite 201, Rockland, MA 02370, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

JW North America, Inc (Owner Number: 10027891)

Owner / Operator Contact Address

200 Ledgewood Place, Suite 201, Rockland, MA 02370, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K152273

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2020-02-25
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2020-02-27
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2020-02-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JW North America, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1054665	JW NORTH AMERICA, INC.	Cartersville, GA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K875190	Ultra Tan Intl. AB	ULTRA TAN PURPLE PRO	1988-01-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1450790. Last updated year: 2026. Please use registration number 1450790 when referencing this establishment in official correspondence.