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Sign in to claim this brandAchimhai Medical Corporation
US
Last updated May 23, 2026
What Achimhai Medical Corporation makes
Achimhai Medical Corporation manufactures dental implants and related components, including screw endosteal dental implants (both one-piece and two-piece designs), as well as preformed suprastructures for both permanent and temporary use. Their portfolio also includes reusable dental drill bits for fixture and appliance applications, designed for dental restoration procedures.
The company’s devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. 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 Achimhai Medical Corporation manufacture?
Achimhai Medical Corporation specializes in dental implants and related components. Their portfolio includes screw endosteal dental implants, available in both one-piece and two-piece designs, as well as preformed suprastructures for permanent and temporary dental restorations. Additionally, they produce reusable dental drill bits for fixture and appliance applications, all of which support dental restoration procedures.
Where is Achimhai Medical Corporation based?
Achimhai Medical Corporation is headquartered in the United States. The company’s location is relevant for regulatory purposes, as it influences compliance requirements and reporting standards for its devices.
Are Achimhai Medical Corporation’s devices listed in any regulatory registries?
Yes, Achimhai Medical Corporation’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and other stakeholders to verify device details such as manufacturer information, model names, and regulatory classifications.
How are Achimhai Medical Corporation’s devices classified under FDA regulations?
Achimhai Medical Corporation’s devices fall under two FDA classification categories: Class I and Class II. The classification depends on factors like the device’s intended use, risk level, and potential impact on patient safety. For example, dental drill bits are typically classified as Class II due to their role in precision procedures, while some implants may qualify as Class I if they pose minimal risk. Classification determines the regulatory pathway and reporting requirements for each device.
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
- 694197900
Catalogue (1280)
Page 3 of 26| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| KISSES Internal Abutment | ATDA6535N | FDA UDI | Class II | Active |
| Kisses Plus Implant System | PFX-5515SD | FDA UDI | Class II | Active |
| Kisses Plus Implant System | KAA45425HB | FDA UDI | Class II | Active |
| Nexplant | I4215M-SH | FDA UDI | Class II | Active |
| KISSES MINI Ball Fixture | MBX-282008S | FDA UDI | Class II | Active |
| Nexplant | I3810M | FDA UDI | Class II | Active |
| KISSES MINI Internal Abutment | KMAA35325H | FDA UDI | Class II | Active |
| KISSES Internal Abutment | ATDA554570H | FDA UDI | Class II | Active |
| Kisses Plus Implant System | PFX-4611SS | FDA UDI | Class II | Active |
| KISSES Internal Fixture | KS5110SA | FDA UDI | Class II | Active |
| Aimgen Max | PFX-3908SS | FDA UDI | Class II | Active |
| Nexplant | MHA3025 | FDA UDI | Class II | Active |
| Kisses Plus Implant System | PFX-5515SS | FDA UDI | Class II | Active |
| KISSES MINI Internal Abutment | KMDA351570H | FDA UDI | Class II | Active |
| Kisses Plus Implant System | KAA55415HB | FDA UDI | Class II | Active |
| Nexplant | I4613 | FDA UDI | Class II | Active |
| KISSES Internal Abutment | ATDA4545N | FDA UDI | Class II | Active |
| Nexplant | S-OTI55SN | FDA UDI | Class I | Active |
| KISSES Internal Abutment | ATSSA48370 | FDA UDI | Class II | Active |
| Aimgen Max | PFX-3813SS | FDA UDI | Class II | Active |
| KISSES MINI Post Fixture | MPX-282511S | FDA UDI | Class II | Active |
| KISSES Internal Abutment | ATDA6545N | FDA UDI | Class II | Active |
| KISSES MINI Internal Fixture | MFX-3213SD | FDA UDI | Class II | Active |
| KISSES Internal Abutment | KSA552570 | FDA UDI | Class II | Active |
| Aimgen Max | KMCS14 | FDA UDI | Class II | Active |
| Nexplant | S-OTI45LN | FDA UDI | Class I | Active |
| Nexplant | S-OTI40SN | FDA UDI | Class I | Active |
| KISSES Internal Abutment | ATDA553570H | FDA UDI | Class II | Active |
| Kisses Plus Implant System | KFX-4215SS | FDA UDI | Class II | Active |
| KISSES Internal Abutment | KDA453555N | FDA UDI | Class II | Active |
| KISSES Internal Abutment | KDA557040H | FDA UDI | Class II | Active |
| Nexplant | I5185M | FDA UDI | Class II | Active |
| KISSES Internal Abutment | ATDA5555N | FDA UDI | Class II | Active |
| Kisses Plus Implant System | KAA45215N | FDA UDI | Class II | Active |
| KISSES Internal Fixture | KS4613SA | FDA UDI | Class II | Active |
| Kisses Plus Implant System | KFX-4208SS | FDA UDI | Class II | Active |
| KISSES Plus Implant System | KCC-M | FDA UDI | Class II | Active |
| KISSES Internal Abutment | KSSA48270 | FDA UDI | Class II | Active |
| KISSES Internal Fixture | KS3810SA | FDA UDI | Class II | Active |
| Aimgen Max | TEDI20L | FDA UDI | Class II | Active |
| Kisses Plus Implant System | PFX-3811SD | FDA UDI | Class II | Active |
| Kisses Plus Implant System | ATAS20 | FDA UDI | Class II | Active |
| KISSES Internal Abutment | KDA553540N | FDA UDI | Class II | Active |
| KISSES MINI Internal Fixture | MFX-3215S | FDA UDI | Class II | Active |
| KISSES MINI Post Fixture | MPX-304008S | FDA UDI | Class II | Active |
| KISSES Plus Implant System | KMS-25 | FDA UDI | Class II | Active |
| ATICON Internal Fixture | AT4514 | FDA UDI | Class II | Active |
| KISSES Internal Fixture | KS5108SA | FDA UDI | Class II | Active |
| KISSES Internal Abutment | ATSA454540 | FDA UDI | Class II | Active |
| Nexplant | SD-2011 | FDA UDI | Class I | Active |
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