SURGICON AG

FDA Device Registration & Listing · St Gallen Sankt Gallen, CH · Registration 3022137228

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022137228
FEI Number
3022137228
Entity Name
SURGICON AG
City/State/Country
St Gallen Sankt Gallen, CH
Establishment Address
Lerchenfeldstrasse 3, St Gallen, St Gallen Sankt Gallen 9014, CH
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
SURGICON AG (Owner Number: 10084629)
Owner / Operator Contact Address
Lerchenfeldstrasse 3, St Gallen, CH-SG 9014, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SURGIFLOW SURGICUT SURGICUT Protect

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYG Device, Irrigation, Ocular Surgery Ophthalmic Class 1 886.4360 2022-09-05
HNN Knife, Ophthalmic Ophthalmic Class 1 886.4350 2022-03-15

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: LIBERTY MANAGEMENT GROUP LTD. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

SURGICON AG
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
K874057 Myocure, Inc. OPHTHALMIC TIP & BLADE SCALPELS 1987-12-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0026-04 Surgical Specialties Corp 1
Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024 Alcon Research LLC Aspex Facility 1
20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024 Alcon Research LLC Aspex Facility 1
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1925-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022137228. Last updated year: 2026. Please use registration number 3022137228 when referencing this establishment in official correspondence.
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