Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2133817

FEI Number

3000210901

Entity Name

WOODWAY USA, INC.

City/State/Country

Vernon, WI, US

Establishment Address

W234n700 Busse Rd, Vernon, WI 53188, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

WOODWAY USA, INC. (Owner Number: 9026547)

Owner / Operator Contact Address

WEST 229 NORTH 591 FOSTER CT., --, Waukesha, WI 53186, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PPS 70 PPS 55 PPS 43 Continuum Pro Med 4Front Med Boost 2 Pro XL Med

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IOL	Treadmill, Powered	Physical Medicine	Class 1	890.5380	1996-09-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WOODWAY USA, INC.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2133817. Last updated year: 2026. Please use registration number 2133817 when referencing this establishment in official correspondence.