Identity

Trade Name
VITA AKZENT FDA UDI
Generic Name
Dental porcelain/ceramic restoration kit FDA UDI
Device Name
VITA Akzent Akz01, 3 g FDA UDI
Model / Reference
BAT013 FDA UDI
Description
VITA Akzent Akz01, 3 g FDA UDI

Identifiers

Primary DI / UDI-DI
J017BAT0130 FDA UDI
510(k) Number
K901982 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental porcelain/ceramic restoration kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 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

No

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 porcelain/ceramic restoration kit

Vita Akzent by Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental porcelain/ceramic restoration kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 186c3eba-deec-4812-9e4e-5a7c0e61d391 35 fields · synced May 29, 2026