Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023878

FEI Number

3023878

Entity Name

BENIK CORP.

City/State/Country

Silverdale, WA, US

Establishment Address

11871 SILVERDALE WAY N.W., No. 107, Silverdale, WA 98383, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BENIK CORP. (Owner Number: 3023860)

Owner / Operator Contact Address

11871 SILVERDALE WAY NW, #107, Silverdale, WA 98383, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BENIK BENIK BENIK BENIK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MRI	Orthosis, Truncal/Orthosis, Limb	Physical Medicine	Class 1	890.3490	2001-11-19
IQQ	Joint, Shoulder, External Limb Component	Physical Medicine	Class 1	890.3420	2001-11-19
ITQ	Joint, Knee, External Brace	Physical Medicine	Class 1	890.3475	2001-11-19
ILH	Splint, Hand, And Components	Physical Medicine	Class 1	890.3475	2001-11-19

Official Correspondent

TIM BAUMGARTNER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BENIK CORP.

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 3023878. Last updated year: 2026. Please use registration number 3023878 when referencing this establishment in official correspondence.