Identity
- Trade Name
- everStick® FDA UDI
- Generic Name
- Dental reinforcing fibre FDA UDI
- Device Name
- everStick® COMBI 1 x 8 cm everStickC&B, 1 x 8 cm everStickPERIO, 1 x 30 cm2 everStickNET, 5x everStick POST, 1 x StickSTEPPER hand instrument, 1 x Stick REFIX D silicone instrument FDA UDI
- Model / Reference
- 900836 FDA UDI
- Description
- everStick® COMBI 1 x 8 cm everStickC&B, 1 x 8 cm everStickPERIO, 1 x 30 cm2 everStickNET, 5x everStick POST, 1 x StickSTEPPER hand instrument, 1 x Stick REFIX D silicone instrument FDA UDI
Identifiers
- Catalog Number
- 900836 FDA UDI
- Primary DI / UDI-DI
- J0229008361 FDA UDI
- FDA Product Code
- EBI FDA UDI
- GMDN Term
- Dental reinforcing fibre FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3760 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental reinforcing fibre
everStick® by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Gc America Inc.
Sources (1)
- FDA UDI ca84f1ee-76e0-4f5b-963a-a08c5ea427b4 36 fields · synced May 31, 2026