Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024706750

FEI Number

3024706750

Entity Name

KERI MEDICAL

City/State/Country

Plan-les-Ouates Geneve, CH

Establishment Address

Chemin du Pre-Fleuri 5, Plan-les-Ouates Geneve 1228, CH

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Keri Medical (Owner Number: 10085771)

Owner / Operator Contact Address

Chemin du Pre-Fleuri 5, Plan-les-Ouates, CH-GE 1228, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K211385

PMA Number

N/A

All Registered Proprietary Names

STARTER Kirschner wire TOUCH INTL tray TOUCH INTL rack lid TOUCH INTL rack TOUCH INTL lid KERIFLEX LID KERIFLEX TRAY Pattern PIP 4 Offset Neck Pattern 6-S Stem Pattern 2 Straight Neck Pattern 8-M Spherical Cup Pattern 9 Spherical Cup Pattern 10 Stem Pattern 3 Conical Cup Pattern 10 Stem Pattern 1 Pattern PIP 3 Pattern PIP 2 Pattern MCP 50 Pattern MCP 00 Pattern MCP 60 Pattern MCP 30 Straight AO Handle Offset Neck Pattern 10-L Conical Cup Pattern 9 Stem Pattern 0 Pattern MCP 40 Pattern MCP 10 K-Wire Centering Guide Stem Pattern 4 Straight Neck Pattern 6-S Stem Pattern XS Offset Neck Pattern 8-M Straight Neck Pattern 10-L Pattern PIP 1 Pattern MCP 20 Pattern PIP 5 PIP DISTAL PROGRESSIVE RASP MCP PROXIMAL PROGRESSIVE RASP MCP DISTAL PROGRESSIVE RASP PIP PROXIMAL PROGRESSIVE RASP KeriFlex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HWD	Starter, Bone Screw	Orthopedic	Class 1	888.4540	2022-09-26
HXI	Passer, Wire, Orthopedic	Orthopedic	Class 1	888.4540	2026-03-19
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2022-09-26
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2022-09-26
GAC	Rasp, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2022-09-26
KYJ	Prosthesis, Finger, Constrained, Polymer	Orthopedic	Class 2	888.3230	2022-09-26

Official Correspondent

Camille Miletto

US Agent Details

Deborah Nilson Business: Nilson Law Group Email: dnilson@nilsonlaw.com Phone: (212) 6871155

Related Public Records

Same Entity

Keri Medical

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
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105

Similar Registrations

Registration Number	Establishment Name	Location
3007125392	Apex (Guangzhou) Tools & Orthopedics Company	Guangzhou Guangdong, CN
1043534	WRIGHT MEDICAL TECHNOLOGY, INC.	Arlington, TN, US
3009790163	AEGIS MEDITEC, INC.	Costa Mesa, CA, US
8040278	Falcon Surgical Co. (Pvt.) Ltd.	Sialkot Punjab, PK
1647149	Steritec Services, LLC	ATHENS, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3024706750. Last updated year: 2026. Please use registration number 3024706750 when referencing this establishment in official correspondence.