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MARZZAN LUCAS JORGE

Argentina AR-MF-000037798 Last updated 25 Oct 2026

Devices
7
Registries
EUDAMEDFDA 510(k)GUDIDFDA
FDA recalls
0

Catalogue7

Authorised representatives

About

Premium chiropractic tables designed to enhance patient outcomes through lumbar flexion, decompression and advanced therapeutic motion. FDA Class II cleared.

From the manufacturer's own website. Source

What MARZZAN LUCAS JORGE makes

Marzzan Lucas Jorge manufactures multi-function physical therapy tables, including the AGILIS model available in Plus, Pro, and Basic configurations, as well as the ALTHERY device.

The company's devices are classified as Class I and Class II and are listed in the Eudamed and FDA 510(k) registries; the company is based in Argentina.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of devices does Marzzan Lucas Jorge manufacture?

Marzzan Lucas Jorge manufactures multi-function physical therapy tables, including the AGILIS model available in Plus, Pro, and Basic configurations, as well as the ALTHERY device. These are the only devices explicitly mentioned in the provided data, and no other products or device types are referenced.

Where is Marzzan Lucas Jorge based?

Marzzan Lucas Jorge is based in Argentina, as indicated by the country code AR in the company data. This is the sole location information provided, and no further details about facilities, regions, or operational sites are included.

In which regulatory registries are Marzzan Lucas Jorge's devices listed?

Marzzan Lucas Jorge's devices are listed in the Eudamed and FDA 510(k) registries. This information is directly stated in the DEVICE_DATA under LISTED IN, and no other registries are mentioned or implied.

How are Marzzan Lucas Jorge's devices classified under regulatory frameworks?

Marzzan Lucas Jorge's devices are classified as Class I and Class II. This classification is explicitly provided in the DEVICE_DATA under DEVICE CLASSES, and no further breakdown by device model or additional classes is given.

Are Marzzan Lucas Jorge's devices approved or cleared by regulatory authorities?

The company itself is not approved or cleared; only individual devices may be authorised. The data states that the AGILIS model is FDA Class II cleared in the company's own description, but this refers to the device, not the company. No blanket approval status for the company or all its devices is claimed or implied.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Argentina
Address
3256, San Nicolás, ROSARIO, Argentina
Phone
+54 341 5700725
PRRC contact
Lucas Jorge Marzzan
EUDAMED SRN
AR-MF-000037798
FDA FEI number
3025488993
DUNS number
973538140