FDA Registration Active 🇨🇭 Switzerland

KERI MEDICAL

Reg #: 3024706750 · FEI: 3024706750 · Expires 2026
Products
9
Proprietary Names
48
Establishment Types
3
Classifications
9

Registration Details

Registration Name
KERI MEDICAL
Registration Number
3024706750
FEI Number
3024706750
Status
Active
Expiry Year
2026
Initial Importer
No
Address
Chemin du Pre-Fleuri 5
City
Plan-les-Ouates Geneve
Country
CH

Regulatory Submissions

510(k) Number
K211385
PMA Number
P240020

Owner / Operator

Firm Name
Keri Medical
Operator Number
10085771
Address
Chemin du Pre-Fleuri 5
City
Plan-les-Ouates
State
Geneve
Postal Code
1228
Country
CH
Correspondent
Camille Miletto

US Agent

Business Name
Nilson Law Group
Contact Name
Deborah Nilson
Address
10 E. 40th Street, Suite 3310
City
New York
State
NY
ZIP
10016
Country
US
Phone
212 6871155

Products

Device Name Product Code
Starter, Bone Screw HWD
Passer, Wire, Orthopedic HXI
Tray, Surgical LRP
Orthopedic Manual Surgical Instrument LXH
Rasp, Surgical, General & Plastic Surgery GAC
Prosthesis, Finger, Constrained, Polymer KYJ
Awl HWJ
Prosthesis, Finger, Semi-Constrained, Metal/Polymer SFA
Tray, Surgical, Instrument FSM

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 Neck holding forceps Snake retractor BONE AWL TOUCH® CMC 1 Kirschner wire Tube

Establishment Types

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