Amparo Prosthetics, Inc.

FDA Device Registration & Listing · West Valley City, UT, US · Registration 3022019579

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022019579
FEI Number
3022019579
Entity Name
Amparo Prosthetics, Inc.
City/State/Country
West Valley City, UT, US
Establishment Address
2111 West Alexander St, West Valley City, UT 84119, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amparo Prosthetics, Inc. (Owner Number: 10084709)
Owner / Operator Contact Address
2111 W Alexander St, West Valley City, UT 84119, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

One-way Valve Resilience Button Valve Kit Pin-lock Unit Confidence Socket Trust Socket Resilience Socket

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISP Valve, Prosthesis Physical Medicine Class 1 890.3420 2023-01-11
IQO Device, Prosthesis Alignment Physical Medicine Class 1 890.3025 2023-01-11
ISS Prosthesis, Thigh Socket, External Component Physical Medicine Class 1 890.3420 2022-03-24

Official Correspondent

Wesley Teerlink

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amparo Prosthetics, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
9616494 Ottobock SE & Co. KGaA formerly known as Otto Bock Healthcare GmbH DUDERSTADT Lower Saxony, DE
3005190268 Otto Bock Healthcare Products GmbH Vienna Wien, AT
3013742611 O AND P DE MEXICO S.A. DE C.V. Guadalajara Jalisco, MX
3018070833 Ottobock Manufacturing Bulgaria EOOD Blagoevgrad, BG
1522166 WillowWood Global LLC Mt Sterling, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022019579. Last updated year: 2026. Please use registration number 3022019579 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.