Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016112541

FEI Number

3016112541

Entity Name

ORTHOPRESS INC.

City/State/Country

Austin, TX, US

Establishment Address

209 E Ben White Blvd Ste 205, Austin, TX 78704, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Orthopress Inc. (Owner Number: 10061768)

Owner / Operator Contact Address

7500 W Hwy 71, Suite 106, Austin, TX 78735, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Finger Press FingerPress

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILH	Splint, Hand, And Components	Physical Medicine	Class 1	890.3475	2019-11-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Orthopress 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 3016112541. Last updated year: 2026. Please use registration number 3016112541 when referencing this establishment in official correspondence.