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OBTURA SPARTAN ENDODONTICS

US

Last updated May 24, 2026

What OBTURA SPARTAN ENDODONTICS makes

The company manufactures ultrasonic dental systems, including handpiece tips for endodontic and periodontal procedures, reusable adaptors for surgical systems, and ultrasonic generators designed for scaling and debridement in dental treatments. Their portfolio also covers complete ultrasonic scaling/debridement systems, combining handpieces and generators for clinical use in dental offices.

All listed devices fall under Class II regulatory classification in the US and are registered in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable US regulatory requirements for dental ultrasonic systems.

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 Obtura Spartan Endodontics manufacture?

Obtura Spartan Endodontics specializes in ultrasonic dental systems. Their product portfolio includes handpiece tips for endodontic and periodontal procedures, reusable adaptors for ultrasonic surgical systems, and ultrasonic generators. They also produce complete ultrasonic scaling and debridement systems, which combine handpieces and generators for use in dental offices. These devices are designed to assist in cleaning and preparing teeth for treatments.

Where is Obtura Spartan Endodontics based, and what regulatory requirements do they follow?

Obtura Spartan Endodontics is based in the United States. As a manufacturer, they develop and produce devices in compliance with applicable US regulatory standards for dental ultrasonic systems. This includes adherence to requirements for device classification, registration, and listing in relevant databases like the FDA’s Unique Device Identifier (UDI) system.

Which regulatory registries or databases list Obtura Spartan Endodontics’ devices?

Obtura Spartan Endodontics’ devices are registered in the FDA’s Unique Device Identifier (UDI) database. This database is used to track and identify medical devices in the United States, ensuring transparency and traceability for regulatory and clinical purposes. The UDI system helps healthcare providers, regulators, and other stakeholders access key information about the devices.

How are Obtura Spartan Endodontics’ devices classified under US regulations?

All of Obtura Spartan Endodontics’ listed devices fall under Class II regulatory classification in the United States. Class II devices are those that pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. This classification applies to their ultrasonic dental systems, including handpieces, generators, and adaptors, as they are intended for procedures like scaling, debridement, and surgical assistance in dental care.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
078371330

Catalogue (74)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Obtura Spartan 932-017
FDA UDI
Class IIActive
Obtura Spartan 930-050
FDA UDI
Class IIActive
Obtura Spartan 931-011
FDA UDI
Class IIActive
Obtura Spartan 932-015
FDA UDI
Class IIActive
Obtura Spartan 931-015
FDA UDI
Class IIActive
Obtura Spartan 941-700
FDA UDI
Class IIActive
Obtura Spartan 932-023
FDA UDI
Class IIActive
Obtura Spartan 932-010
FDA UDI
Class IIActive
Obtura Spartan 932-008
FDA UDI
Class IIActive
Obtura Spartan 930-014
FDA UDI
Class IIActive
Obtura Spartan 930-016
FDA UDI
Class IIActive
Obtura Spartan 932-014
FDA UDI
Class IIActive
Obtura Spartan 932-018
FDA UDI
Class IIActive
Obtura Spartan 952-615
FDA UDI
Class IIActive
Obtura Spartan 948-201
FDA UDI
Class IIActive
Obtura Spartan 932-006
FDA UDI
Class IIActive
Obtura Spartan 931-116
FDA UDI
Class IIActive
Obtura Spartan 931-013
FDA UDI
Class IIActive
Obtura Spartan 930-018
FDA UDI
Class IIActive
Obtura Spartan 930-017
FDA UDI
Class IIActive
Obtura Spartan 930-046
FDA UDI
Class IIActive
Obtura Spartan 932-013
FDA UDI
Class IIActive
Obtura Spartan 932-016
FDA UDI
Class IIActive
Obtura Spartan 941-600
FDA UDI
Class IIActive
Obtura Spartan 930-012
FDA UDI
Class IIActive
Obtura Spartan 941-100
FDA UDI
Class IIActive
Obtura Spartan 941-400
FDA UDI
Class IIActive
Obtura Spartan 930-608
FDA UDI
Class IIActive
Obtura Spartan 941-157
FDA UDI
Class IIActive
Obtura Spartan 941-104
FDA UDI
Class IIActive
Obtura Spartan 930-033
FDA UDI
Class IIActive
Obtura Spartan 943-710
FDA UDI
Class IIActive
Obtura Spartan 941-106
FDA UDI
Class IIActive
Obtura Spartan 930-115
FDA UDI
Class IIActive
Obtura Spartan 941-500
FDA UDI
Class IIActive
Obtura Spartan 932-024
FDA UDI
Class IIActive
Obtura Spartan 932-020
FDA UDI
Class IIActive
Obtura Spartan 941-109
FDA UDI
Class IIActive
Obtura Spartan 932-019
FDA UDI
Class IIActive
Obtura Spartan 941-101
FDA UDI
Class IIActive
Obtura Spartan 930-034
FDA UDI
Class IIActive
Obtura Spartan 930-043
FDA UDI
Class IIActive
Obtura Spartan 931-016
FDA UDI
Class IIActive
Obtura Spartan 941-147
FDA UDI
Class IIActive
Obtura Spartan 930-015
FDA UDI
Class IIActive
Obtura Spartan 932-004
FDA UDI
Class IIActive
Obtura Spartan 932-003
FDA UDI
Class IIActive
Obtura Spartan 941-105
FDA UDI
Class IIActive
Obtura Spartan 930-041
FDA UDI
Class IIActive
Obtura Spartan 930-031
FDA UDI
Class IIActive

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