ZURIMED TECHNOLOGIES AG

FDA Device Registration & Listing · Zurich, CH · Registration 3034932459

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
3034932459
FEI Number
3034932459
Entity Name
ZURIMED TECHNOLOGIES AG
City/State/Country
Zurich, CH
Establishment Address
Lengghalde 5, Zurich 8008, CH
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
ZuriMED Technologies AG (Owner Number: 10092442)
Owner / Operator Contact Address
Lengghalde 5, Zurich, CH-ZH 8008, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

FiberLocker PowerUnit Transfer Shield PowerUnit Motor Pack FiberLocker PowerUnit Handpiece FiberLocker PowerUnit Motor Pack PowerUnit Handpiece FiberLocker PowerUnit PowerUnit Transfer Shield PowerUnit Charging Station FiberLocker PowerUnit Charging Station FiberLocker Implant FiberLocker Instrument SpeedPatch PET FiberLocker System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment General, Plastic Surgery Class 1 878.4820 2026-01-20
OWX Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon General, Plastic Surgery Class 2 878.3300 2025-01-08

Official Correspondent

Elias Bachmann

US Agent Details

Veronica Besmer Email: veronica@besmer.com Phone: (415) 4411775

Related Public Records

Same Entity

ZuriMED Technologies 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
K933337 R & D Batteries, Inc. R AND D BATTERY REPLACEMENT 1994-04-05
K873766 Bowen & Company, Inc. STERNAL POWER AWL 1988-11-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034932459. Last updated year: 2026. Please use registration number 3034932459 when referencing this establishment in official correspondence.
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