Identity
- Trade Name
- AIMGEN MAX FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- AIMGEN MAX Transfer Impression Coping Φ3.5 FDA UDI
- Model / Reference
- KMIT35H FDA UDI
- Description
- AIMGEN MAX Transfer Impression Coping Φ3.5 FDA UDI
Identifiers
- Catalog Number
- MIT-35HL-PA FDA UDI
- Primary DI / UDI-DI
- 08800024953892 FDA UDI
- 510(k) Number
- K142813 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental implant suprastructure, temporary, preformed, single-use
Aimgen Max by Achimhai Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, temporary, preformed, single-use.
- Intraoral Scanbody — ARUM DENTISTRY Co., Ltd. · Class I
- Impression Coping — ARUM DENTISTRY Co., Ltd. · Class I
- Intraoral Scanbody — ARUM DENTISTRY Co., Ltd. · Class I
- Retaining Screw for Digital Model Analog — ADIN DENTAL IMPLANT SYSTEMS LTD. · Class I
- Falcon — Falcon Surgical Co. (Pvt.) Ltd · Class I
- Impression Coping — ARUM DENTISTRY Co., Ltd. · Class I
- Neoss Implant System — Neoss, Ltd. · Class II
- Scanbody Screw — ARUM DENTISTRY Co., Ltd. · Class I
Cleared under the same submission
K142813 also covers:
- AIMGEN MAX — Achimhai Medical Corporation
- AIMGEN MAX — Achimhai Medical Corporation
- AIMGEN MAX — Achimhai Medical Corporation
- AIMGEN MAX — Achimhai Medical Corporation
- AIMGEN MAX — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
- KISSES Internal Abutment — Achimhai Medical Corporation
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Achimhai Medical Corporation
Sources (1)
- FDA UDI 47743860-22f9-40f7-803b-d70ede40e469 36 fields · synced Jun 8, 2026