Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013051157

FEI Number

3013051157

Entity Name

PAUL BUETIGER AG

City/State/Country

Biberist Solothurn, CH

Establishment Address

Solothurnstrasse 57, Biberist Solothurn 4562, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Paul Buetiger AG (Owner Number: 10077930)

Owner / Operator Contact Address

Solothurnstrasse 57, Biberist, CH-NOTA 4562, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Surgical Templates

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HWT	Template	Orthopedic	Class 1	888.4800	2020-10-06

Official Correspondent

Lukas Buetiger

US Agent Details

Alfred Lerch Business: confinis USA Inc. Email: usagent@confinis.com Phone: (910) 2289391

Related Public Records

Same Entity

Paul Buetiger 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 3013051157. Last updated year: 2026. Please use registration number 3013051157 when referencing this establishment in official correspondence.