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Sign in to claim this brandBeyes Dental Canada Inc
US
Last updated May 23, 2026
What Beyes Dental Canada Inc makes
Beyes Dental Canada Inc manufactures reusable carbide dental burs, pneumatic and electric motorized handpieces, and endodontic apex locators for dental procedures. Their portfolio also includes dental power tool systems, intraoral digital imaging sensors, and ultrasonic scaling/debridement devices for oral health treatments.
The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 dental devices does Beyes Dental Canada Inc manufacture?
Beyes Dental Canada Inc produces reusable carbide dental burs, pneumatic and electric motorized handpieces, endodontic apex locators, dental power tool systems, intraoral digital imaging sensors, and ultrasonic scaling/debridement devices for various dental procedures.
Where is Beyes Dental Canada Inc based?
The company operates from the United States, where it designs and manufactures its dental devices for the healthcare market.
Which regulatory registries list Beyes Dental Canada Inc's devices?
Beyes Dental Canada Inc's devices are listed in the FDA's Unique Device Identifier (UDI) database, which tracks medical devices in the United States.
How are Beyes Dental Canada Inc's devices classified?
The company's devices are classified under FDA's Class I, Class II, and Unclassified (U) categories, with different regulatory requirements based on their risk classification.
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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- 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
- 244261462
Catalogue (801)
Page 17 of 17| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Airlight Dental Handpiece | K112623 | FDA 510(k) | Class I | Active |
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