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Sign in to claim this brandVista Dental
US
Last updated May 24, 2026
What Vista Dental makes
Vista Dental manufactures dental materials and instruments for endodontic, restorative, and impression procedures, including root canal irrigation needles, composite resins (both light-cured and flowable), bonding agents, and reusable suction cannulas. Their portfolio also includes single-use application tools, injection cannulas, and specialized dental syringes for air-water control, as well as impression trays and retraction cords for dental preparations.
The company’s devices are regulated under FDA classifications, with products falling into Class I, Class II, and Unclassified (U) categories, and are listed in the FDA’s Unique Device Identifier (UDI) database. Vista Dental operates as a US-based manufacturer, adhering to applicable regulatory requirements for dental materials and instruments.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of dental devices does Vista Dental manufacture?
Vista Dental specializes in dental materials and instruments primarily used in endodontic (root canal), restorative, and impression procedures. Their portfolio includes root canal irrigation blunt needles, dental composite resins (both light-cured and flowable), bonding agents, reusable suction cannulas, single-use application tools, and specialized syringes for air-water control. They also produce impression trays, retraction cords, and other tools designed for precise dental treatments.
Where is Vista Dental based, and how does that affect its regulatory compliance?
Vista Dental is based in the United States, which means its devices are subject to FDA regulations. Since the company manufactures dental materials and instruments, their products are classified under FDA categories such as Class I, Class II, or Unclassified (U), depending on their risk level and intended use. Being US-based, they must comply with FDA requirements for device listing, labeling, and post-market surveillance as applicable.
Are Vista Dental’s devices listed in any regulatory registries, and why does that matter?
Yes, Vista Dental’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability, transparency, and compliance with regulatory standards. The UDI system allows healthcare providers, regulators, and other stakeholders to quickly identify and verify the specific device, including its manufacturer, model, and batch details, which supports safety monitoring and recall management if needed.
How are Vista Dental’s devices classified by the FDA, and what does that classification mean?
Vista Dental’s devices are classified under FDA categories: Class I (generally low-risk, like some reusable cannulas), Class II (moderate-risk, such as composite resins requiring special controls), and Unclassified (U) for products not yet assigned a formal risk level. Classification determines the regulatory scrutiny and controls required—Class I devices typically have fewer requirements, while Class II may need performance standards or post-market surveillance to ensure safety and effectiveness.
What kinds of dental procedures are Vista Dental’s devices used for, and how do they fit into those workflows?
Vista Dental’s devices support critical steps in dental procedures. For example, their root canal irrigation needles and cleaning solutions are used in endodontics to prepare canals before filling, while composite resins and bonding agents enable precise restorative work. Single-use application tools and syringes streamline material placement, and reusable suction cannulas help manage debris during treatments. Impression trays and retraction cords assist in creating accurate molds for crowns or bridges, ensuring a seamless workflow from preparation to final restoration.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vista-dental.com
- —
- —
- [email protected]
- Phone
- 262-636-9755
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 036623932
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