Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017860875

FEI Number

3017860875

Entity Name

PRECXIS

City/State/Country

Peillonnex Haute-Savoie, FR

Establishment Address

1200 Route de Findrol, Bat B, Peillonnex Haute-Savoie 74250, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PRECXIS (Owner Number: 10079521)

Owner / Operator Contact Address

Chemin de la Foret, Peillonnex, FR-74 74250, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Neofuse Percutaneous Burrs KONTACT DENTAL IMPLANT SYSTEM Neomis ANT kit Drill bits (reamer)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXX	Screwdriver	Orthopedic	Class 1	888.4540	2025-04-01
GFF	Bur, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4820	2022-02-15
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2020-12-10
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2024-11-26
GFG	Bit, Surgical	General, Plastic Surgery	Class 1	878.4820	2024-11-26

Official Correspondent

Thomas Teille

US Agent Details

Christine Scifert Business: MRC GLOBAL LLC Email: christine.scifert@askmrcglobal.com Phone: (901) 8318053

Related Public Records

Same Entity

PRECXIS

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
1417592	MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, US
3009959868	Ferry Machine Corporation	Little Ferry, NJ, US
8010916	Kammerer Medical Systems GmbH & Co. KG	Stockach Baden-Wurttemberg, DE
3007689689	ELOS MEDTECH PINOL A/S	Goerloese Hovedstaden, DK
1038671	EXACTECH, INC.	GAINESVILLE, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017860875. Last updated year: 2026. Please use registration number 3017860875 when referencing this establishment in official correspondence.