Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8043872

FEI Number

3002807219

Entity Name

HOFMANN S.R.L.

City/State/Country

MONZA (MI) Monza e Brianza, IT

Establishment Address

VIA CARLO CARRA 19, MONZA (MI) Monza e Brianza 20900, IT

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

HOFMANN S.R.L. (Owner Number: 9004217)

Owner / Operator Contact Address

VIA CARLO CARRA 19, --, MONZA (MI), IT-MB 20900, IT

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
JDW	Pin, Fixation, Threaded	Orthopedic	Class 2	888.3040	2007-12-11

Official Correspondent

No official correspondent registered.

US Agent Details

Barry Sands Business: Regulatory/Quality Management Information Source, Inc. Email: fdaadminsupport@rqmis.com Phone: (978) 8345701

Related Public Records

Same Entity

HOFMANN S.R.L.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K223112	Smith & Nephew, Inc.	MAVERICK Mini External Fixation System	2022-12-08

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1043653	ONYX MEDICAL LLC	MEMPHIS, TN, US
1043534	WRIGHT MEDICAL TECHNOLOGY, INC.	Arlington, TN, US
1221934	DePuy Mitek, Inc.	RAYNHAM, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043872. Last updated year: 2026. Please use registration number 8043872 when referencing this establishment in official correspondence.