Is this your brand? Sign in to claim ownership.
Sign in to claim this brandAETON MEDICAL
US
Last updated September 17, 2026
What AETON MEDICAL makes
Aeton Medical manufactures dental implant suprastructures, including both preformed single-use and custom-made temporary options. Their product portfolio also features dental implant abutment impression caps, analogs, surgical kits, and single-use dental prosthesis abutment screw analogs.
The company is based in the United States, and its products are classified as Class II medical devices. These devices are listed within the FDA UDI database.
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 Aeton Medical manufacture?
Aeton Medical specializes in dental implant-related devices. Their portfolio includes temporary dental implant suprastructures (both preformed single-use and custom-made), dental implant abutment impression caps, analogs, surgical kits, and single-use dental prosthesis/implant abutment screw analogs. These products support various stages of dental implant procedures, from initial placement to final restoration.
Where is Aeton Medical based, and what country regulates its devices?
Aeton Medical is based in the United States. Since their devices fall under FDA jurisdiction, they are subject to U.S. regulatory requirements, including classification and listing in the FDA’s Unique Device Identifier (UDI) database.
How are Aeton Medical’s devices classified by regulatory authorities?
Aeton Medical’s devices are classified as Class II medical devices. This classification typically applies to products that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as dental implant components that require validation of performance and biocompatibility.
Are Aeton Medical’s devices listed in any regulatory registries?
Yes, Aeton Medical’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices in the U.S., allowing healthcare providers, regulators, and patients to verify product details, including manufacturer information and device classification.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 7115 Airport Hwy, Pennsauken, NJ, 08109
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3007536957
- DUNS Number
- —
Catalogue (66)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Aeton Medical | STHC484 | FDA UDI | Class II | Active |
| Aeton Medical | AMSTAS485 | FDA UDI | Class II | Active |
| Aeton Medical | BNBH404 | FDA UDI | Class II | Active |
| Aeton Medical | STIC48 | FDA UDI | Class II | Active |
| Aeton Medical | STICA484 | FDA UDI | Class II | Active |
| Aeton Medical | STAN655 | FDA UDI | Class II | Active |
| Aeton Medical | BRCH603 | FDA UDI | Class II | Active |
| Aeton Medical | STHC652 | FDA UDI | Class II | Active |
| Aeton Medical | BRBH704 | FDA UDI | Class II | Active |
| Aeton Medical | AMSTAS487 | FDA UDI | Class II | Active |
| Aeton Medical | AMSTAS654 | FDA UDI | Class II | Active |
| Aeton Medical | STAN485 | FDA UDI | Class II | Active |
| Aeton Medical | STICA654 | FDA UDI | Class II | Active |
| Aeton Medical | BNBH505 | FDA UDI | Class II | Active |
| Aeton Medical | BRCH604 | FDA UDI | Class II | Active |
| Aeton Medical | BNCH485 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.