Identity

Trade Name
VITAPAN FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
VITAPAN Anteriores, MON, L11, Lehrzähne FDA UDI
Model / Reference
A6MONL11 FDA UDI
Description
VITAPAN Anteriores, MON, L11, Lehrzähne FDA UDI

Identifiers

Primary DI / UDI-DI
J017A6MONL110 FDA UDI
510(k) Number
K914476 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Resin artificial teeth

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

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7119ca1b-d078-44c3-a718-83238b79bb7d 35 fields · synced Jun 1, 2026