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MECTRON SPA

US

Last updated May 24, 2026

What MECTRON SPA makes

The company produces dental ultrasonic surgical systems and associated handpiece tips, including periodontal, endodontic, and hard-tissue variants. These devices are designed for surgical precision, scaling, debridement, and torque adjustment in dental procedures. Reusable torque wrenches for ultrasonic systems are also part of the portfolio.

The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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

Frequently asked questions

What types of medical devices does MECTRON SPA manufacture?

MECTRON SPA specializes in dental ultrasonic surgical systems and their associated components. This includes handpiece tips for surgical precision (such as periodontal and hard-tissue variants), ultrasonic scaling/debridement systems (including endodontic tips), and full ultrasonic surgical systems. The company also produces reusable torque wrenches designed for use with ultrasonic dental systems, ensuring precise torque control during procedures.

Where is MECTRON SPA based, and does it operate internationally?

MECTRON SPA is headquartered in the United States. While the company’s primary location is in the US, its devices may be distributed or used globally depending on regulatory compliance and market demand. The company’s focus is on dental ultrasonic systems, which are widely applicable in clinical settings worldwide.

Which regulatory registries or databases list MECTRON SPA’s devices?

MECTRON SPA’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, allowing them to verify and track specific models of ultrasonic dental systems and accessories. Listing in the UDI database is a requirement for Class I and Class II devices under FDA regulations.

How are MECTRON SPA’s devices classified under FDA regulations?

MECTRON SPA’s devices fall into two FDA classification categories: Class I and Class II. Class I devices are generally considered low-risk and typically require only general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the nature of the procedure it supports, such as ultrasonic scaling or surgical precision in dentistry.

What is the purpose of the ultrasonic surgical systems and handpiece tips produced by MECTRON SPA?

MECTRON SPA’s ultrasonic surgical systems and handpiece tips are designed for high-precision dental procedures, including scaling, debridement, and surgical interventions. Ultrasonic technology enables efficient removal of plaque and calculus, as well as precise cutting or shaping of hard dental tissues. The specialized tips (periodontal, endodontic, or hard-tissue) cater to specific clinical needs, while reusable torque wrenches ensure consistent performance during adjustments, enhancing both accuracy and patient care.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1 6144594922
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
436664734

Catalogue (310)

Page 3 of 7
DeviceModel / ReferenceRegistriesClassStatus
Mectron MT4-20 +
FDA UDI
Class IActive
Mectron PP1
FDA UDI
Class IIActive
Mectron OT5B -US
FDA UDI
Class IIActive
Mectron OP6A -US
FDA UDI
Class IIActive
Mectron MD3-16
FDA UDI
Class IActive
Mectron MT2R-4
FDA UDI
Class IActive
Mectron P14 + K10
FDA UDI
Class IIActive
Mectron P2
FDA UDI
Class IIActive
Mectron PD0223B -US-
FDA UDI
Class IIActive
Mectron OT14 -US
FDA UDI
Class IIActive
Mectron IM2A-15
FDA UDI
Class IIActive
Mectron D4 + K10
FDA UDI
Class IIActive
Mectron MULTIPIEZO -easy -US-
FDA UDI
Class IIActive
Mectron PS1
FDA UDI
Class IIActive
Mectron MT4-10 +
FDA UDI
Class IActive
Mectron PL3
FDA UDI
Class IIActive
Mectron EN6L
FDA UDI
Class IIActive
Mectron W4-H
FDA UDI
Class IIActive
Mectron EL3
FDA UDI
Class IIActive
Mectron IM1S -US
FDA UDI
Class IIActive
Mectron PIEZOSURGERY WHITE
FDA UDI
Class IIActive
Mectron PD0223A -US-
FDA UDI
Class IIActive
Mectron ER5
FDA UDI
Class IIActive
Mectron MF4
FDA UDI
Class IActive
Mectron P15 + K10
FDA UDI
Class IIActive
Mectron OT5 -US
FDA UDI
Class IIActive
Mectron OT9 -US
FDA UDI
Class IIActive
Mectron OP4 -US
FDA UDI
Class IIActive
Mectron PD0432A
FDA UDI
Class IIActive
Mectron TIP IC1 (5 PCS) -US-
FDA UDI
Class IIActive
Mectron MF0804+
FDA UDI
Class IIActive
Mectron IM1 AL -US
FDA UDI
Class IIActive
Mectron MANIPOLO PIEZOSURGERY® medical +
FDA UDI
Class IIActive
Mectron PIEZOSURGERY GP
FDA UDI
Class IIActive
Mectron PIEZOSURGERY TOUCH
FDA UDI
Class IIActive
Mectron ER4 + K10
FDA UDI
Class IIActive
Mectron OT7
FDA UDI
Class IIActive
Mectron LED SCALER HANDPIECE
FDA UDI
Class IIActive
Mectron SLS
FDA UDI
Class IIActive
Mectron OT7-20
FDA UDI
Class IIActive
Mectron PL1
FDA UDI
Class IIActive
Mectron PIEZOSURGERY FLEX -US
FDA UDI
Class IActive
Mectron IM3P-15
FDA UDI
Class IIActive
Mectron RD5 + K10
FDA UDI
Class IIActive
Mectron MT1204
FDA UDI
Class IIActive
Mectron S6
FDA UDI
Class IIActive
Mectron MDI 1.9 -US
FDA UDI
Class IIActive
Mectron P3
FDA UDI
Class IIActive
Mectron SCALER HANDPIECE
FDA UDI
Class IIActive
Mectron OP8 -US
FDA UDI
Class IIActive

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