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Sign in to claim this brandGarrison Dental Solutions LLC
United States·US-MF-000004112
Last updated September 18, 2026
About
Explore Garrison Dental’s industry-leading matrix systems and instruments designed to advance efficiency, precision, and outcomes in restorative dentistry.
From the manufacturer's own website. Source
What Garrison Dental Solutions LLC makes
Garrison Dental Solutions LLC manufactures dental finishing and polishing instruments, including interproximal finishing strips for contouring dental restorations and intra-oral adjustment tools for zirconia-based dental restorations. Their product line also includes clear interproximal wedges for dental spacing and alignment adjustments.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s 510(k) registry. They are also registered in the EU’s eudamed database, reflecting compliance with relevant dental device regulations. The manufacturer 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 dental devices does Garrison Dental Solutions LLC manufacture?
Garrison Dental Solutions LLC specializes in dental finishing and polishing instruments. Their product line includes interproximal finishing strips (like FitStrip™) for contouring dental restorations, intra-oral adjustment tools (such as eZr™) for refining zirconia-based restorations, and clear interproximal wedges (WedgeWands®) used for spacing and alignment adjustments in restorative dentistry. These tools are designed to improve precision and efficiency in dental procedures.
Where is Garrison Dental Solutions LLC based, and what does that mean for regulatory compliance?
Garrison Dental Solutions LLC is based in the United States. This means their devices must comply with U.S. FDA regulations, including classification under FDA’s Class I or Class II categories, and registration in the FDA’s 510(k) database for Class II devices. Additionally, their devices are listed in the EU’s eudamed database, indicating they meet EU dental device regulations, though this does not imply direct EU market authorization without further context.
Which regulatory registries list Garrison Dental Solutions LLC’s devices?
Garrison Dental Solutions LLC’s devices are listed in two key regulatory registries: the FDA’s 510(k) database (for Class II devices) and the EU’s eudamed database. These registries track compliance with U.S. and EU dental device regulations, respectively, ensuring transparency for healthcare providers and authorities. Listing in these databases does not confirm market authorization but reflects regulatory engagement.
How are Garrison Dental Solutions LLC’s devices classified under U.S. regulations?
Garrison Dental Solutions LLC’s devices are classified under the FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway for authorization, such as the 510(k) process for Class II devices, though individual devices must still meet specific criteria for clearance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 150 , Dewitt Lane, Spring Lake, Michigan, United States
- Website
- www.garrisondental.com
- facebook.com/garrisondentalsolutions
- [email protected]
- Phone
- +1-888-437-0032
- PRRC Contact
- Nadia Bishop
- EUDAMED SRN
- US-MF-000004112
- FDA FEI Number
- —
- DUNS Number
- —
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