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ProVecta 3D Prime Ceph

FDA UDI

Class II (US FDA UDI)

by Dürr Dental Se

Identity

Trade Name
ProVecta 3D Prime Ceph FDA UDI
Generic Name
Cone beam computed tomography system, head/neck FDA UDI
Device Name
X-Ray System FDA UDI
Model / Reference
A7861 FDA UDI
Description
X-Ray System FDA UDI

Identifiers

Primary DI / UDI-DI
E247A78610 FDA UDI
510(k) Number
K193139 FDA UDI
K232487 FDA UDI
FDA Product Code
OAS FDA UDI
GMDN Term
Cone beam computed tomography system, head/neck FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cone beam computed tomography system, head/neck

ProVecta 3D Prime Ceph by Dürr Dental Se — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cone beam computed tomography system, head/neck.

Cleared under the same submission

K232487 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dürr Dental Se

Sources (1)

  • FDA UDI b8691eae-0a2c-4505-a47c-e794eef426af 34 fields · synced Jun 8, 2026