Identity
- Trade Name
- Dalbo®-Z FDA UDI
- Generic Name
- Dental anchor FDA UDI
- Device Name
- Dalbo®-Z OE FDA UDI
- Model / Reference
- 050398 FDA UDI
- Description
- Dalbo®-Z OE FDA UDI
Identifiers
- Catalog Number
- 050398 FDA UDI
- Primary DI / UDI-DI
- 07640166513766 FDA UDI
- FDA Product Code
- EJX FDA UDI
- GMDN Term
- Dental anchor FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3130 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental anchor
Dalbo®-Z by Cendres+Métaux SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental anchor.
- IMTEC — Park Dental Research Corp · Class I
- Keystone Industries — Keystone Industries · Class I
- IMTEC — Park Dental Research Corp · Class I
- Keystone Industries — Keystone Industries · Class I
- FRIADENT® — Dentsply Implants Manufacturing GmbH · Class II
- Preat — PREAT Corporation · Class I
- IMTEC — Park Dental Research Corp · Class I
- CEKA & PRECI-LINE ATTACHMENTS — Alpha-Dent · 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
- Cendres+Métaux SA
Sources (1)
- FDA UDI a2c885cc-9bd8-44be-baf4-3deb6b4c4b11 36 fields · synced May 31, 2026