Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010303773

FEI Number

3010303773

Entity Name

NOVENTA AG

City/State/Country

Diepoldsau Sankt Gallen, CH

Establishment Address

Sonnenstrasse 1, Diepoldsau Sankt Gallen 9444, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Noventa AG (Owner Number: 10092832)

Owner / Operator Contact Address

Sonnenstrasse 1, Diepoldsau, CH-SG 9444, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2025-02-24

Official Correspondent

Nieves Bertsch

US Agent Details

Robert Brooks Business: Sigvaris Inc. Email: robert.brooks@sigvaris.com Phone: (770) 6322950

Related Public Records

Same Entity

Noventa AG

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 3010303773. Last updated year: 2026. Please use registration number 3010303773 when referencing this establishment in official correspondence.