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Rebilda Post

FDA UDI

Class I (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
Rebilda Post FDA UDI
Generic Name
Pin/post dental drill bit FDA UDI
Device Name
Endodontic post build-up for support and anchorage of coronal restoration in situations with insufficient tooth substance. FDA UDI
Model / Reference
1771 FDA UDI
Description
Endodontic post build-up for support and anchorage of coronal restoration in situations with insufficient tooth substance. FDA UDI

Identifiers

Catalog Number
1771 FDA UDI
Primary DI / UDI-DI
E22117711 FDA UDI
FDA Product Code
EKS FDA UDI
DZA FDA UDI
ELR FDA UDI
EBF FDA UDI
KLE FDA UDI
EHQ FDA UDI
GMDN Term
Pin/post dental drill bit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
872.4130 FDA UDI
872.3810 FDA UDI
872.3690 FDA UDI
872.3200 FDA UDI
872.3360 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

Yes

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

No

FDA UDI

Category: Dental composite resinDentine bonding agent/setRoot canal post, preformedDental matrix band, single-use

Rebilda Post by VOCO GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin/post dental drill bit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI bd96c2c2-efad-489b-8f31-7a35490de418 36 fields · synced May 31, 2026