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Sign in to claim this brandBuckeye Medical Technologies, LLC
US
Last updated May 26, 2026
What Buckeye Medical Technologies, LLC makes
Buckeye Medical Technologies, LLC manufactures preformed, single-use dental implant suprastructures designed for temporary use during implant procedures. These devices are intended to provide immediate prosthetic support while the final restoration is fabricated.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance and the FDA’s Unique Device Identification (UDI) system. 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 medical devices does Buckeye Medical Technologies, LLC primarily manufacture?
Buckeye Medical Technologies, LLC specializes in dental implant suprastructures that are preformed and designed for single-use. These devices are specifically intended for temporary prosthetic support during dental implant procedures, ensuring stability while the final restoration is being created. The focus is on immediate, short-term solutions in implant dentistry.
Where is Buckeye Medical Technologies, LLC based, and how does that affect its regulatory standing?
Buckeye Medical Technologies, LLC is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies these products as Class II medical devices, which requires compliance with specific controls to ensure safety and effectiveness before market authorization.
Which regulatory registries or databases list Buckeye Medical Technologies, LLC’s devices?
Buckeye Medical Technologies, LLC’s devices are listed in the FDA’s 510(k) clearance database, which documents premarket submissions for Class II medical devices. Additionally, the company’s products are included in the FDA’s Unique Device Identification (UDI) system, ensuring traceability and transparency in the supply chain for these temporary dental implant suprastructures.
How are Buckeye Medical Technologies, LLC’s devices classified under regulatory standards?
Buckeye Medical Technologies, LLC’s dental implant suprastructures fall under the FDA’s Class II medical device classification. This classification is determined based on the level of risk associated with the product—Class II devices require special controls beyond general controls to mitigate risks, such as performance standards or post-market surveillance, before they can be authorized for use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- anatotemp.com
- —
- —
- [email protected]
- Phone
- 3306090386
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 080134511
Catalogue (75)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Anatotemp | 1057-05 | FDA UDI | Class II | Active |
| Anatotemp | 1035-02 | FDA UDI | Class II | Active |
| Anatotemp | 1530-03 | FDA UDI | Class II | Active |
| Anatotemp | 1530-01SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1057-06 | FDA UDI | Class II | Active |
| Anatotemp | 4048-06 | FDA UDI | Class II | Active |
| Anatotemp | 1045-03SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1045-01SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1057-05SCtb | FDA UDI | Class II | Active |
| Anatotemp | 2035-02 | FDA UDI | Class II | Active |
| Anatotemp | 1035-02SCtb | FDA UDI | Class II | Active |
| Anatotemp | 2060-06 | FDA UDI | Class II | Active |
| Anatotemp | 2035-01 | FDA UDI | Class II | Active |
| Anatotemp | 1035-04SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1035-03SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1544-05SCtb | FDA UDI | Class II | Active |
| Anatotemp | 2035-03 | FDA UDI | Class II | Active |
| Anatotemp | 1530-01 | FDA UDI | Class II | Active |
| Anatotemp | 1534-06SCtb | FDA UDI | Class II | Active |
| Anatotemp | 2050-06 | FDA UDI | Class II | Active |
| Anatotemp | 1530-03SCtb | FDA UDI | Class II | Active |
| Anatotemp | 4041-04 | FDA UDI | Class II | Active |
| Anatotemp | 1534-04SCtb | FDA UDI | Class II | Active |
| Anatotemp | 1534-05SCtb | FDA UDI | Class II | Active |
| Anatotemp Anatomic Dental Implant Healing Abutment | K171922 | FDA 510(k) | Class II | Active |
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