Identity
- Trade Name
- DIO Guide Sinus Approach Stopper FDA UDI
- Generic Name
- Dental instrument depth limiter FDA UDI
- Model / Reference
- GST 10YE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800049307465 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental instrument depth limiter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental instrument depth limiter
DIO Guide Sinus Approach Stopper by DIO Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Neoss Implant System — Neoss, Ltd. · Class I
- DIO Sinus Approach Stopper — DIO Corporation · 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 |
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Manufacturer
- Manufacturer
- DIO Corporation
Sources (1)
- FDA UDI 6ac6d00e-9d60-440a-ae45-e3295d4852c9 32 fields · synced May 30, 2026