Identity
- Trade Name
- IOC-USB Cable FDA UDI
- Generic Name
- Intraoral camera FDA UDI
- Device Name
- Accessories of Intraoral Camera FDA UDI
- Model / Reference
- IOC-USB Cable FDA UDI
- Description
- Accessories of Intraoral Camera FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800096901036 FDA UDI
- FDA Product Code
- KQM FDA UDI
- GMDN Term
- Intraoral camera FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Intraoral camera
IOC-USB Cable by Dentall Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intraoral camera.
- Iris — Digital Doc LLC · Class I
- A-dec — A-Dec, Inc. · Class II
- Osstem Implant Co., Ltd. — OSSTEM IMPLANT Co., Ltd. · Class II
- PXL — Digital Doc LLC · Class I
- APOZA — APOZA ENTERPRISE CO., LTD. · Class I
- AIOBIO — AIOBIO Co., Ltd. · Class I
- CamX Spectra Interchangeable Head — DÜRR DENTAL SE · Class II
- RealCloud HD1 — REALCLOUD IMAGING, INC. · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dentall Corporation
Sources (1)
- FDA UDI b97eb027-79a6-4dda-90b6-4f8c8e3f295d 33 fields · synced May 30, 2026