LIZARD INNOVATION GMBH

FDA Device Registration & Listing · Donaueschingen Baden-Wurttemberg, DE · Registration 3042235752

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
3042235752
FEI Number
3042235752
Entity Name
LIZARD INNOVATION GMBH
City/State/Country
Donaueschingen Baden-Wurttemberg, DE
Establishment Address
Karlsplatz 2, Donaueschingen Baden-Wurttemberg 78166, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Lizard Innovation GmbH (Owner Number: 10094136)
Owner / Operator Contact Address
Karlsplatz 2, Donaueschingen, DE-BW 78166, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2025-11-17
GAD Retractor General, Plastic Surgery Class 1 878.4800 2025-11-17
HTR Rasp General, Plastic Surgery Class 1 878.4800 2025-11-17
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2025-11-17

Official Correspondent

Tina Werner

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Lizard Innovation GmbH
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
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19
K820290 The Anspach Effort, Inc. SELF RETAINING RETRACTOR FOR HAND SURG 1982-03-05
K760422 Cutter Laboratories, Inc. SURGICAL RETRACTOR 1976-08-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2014 Aesculap, Inc. 1
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

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8043496 REDA INSTRUMENTE GMBH TUTTLINGEN Baden-Wurttemberg, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042235752. Last updated year: 2026. Please use registration number 3042235752 when referencing this establishment in official correspondence.
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