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Xios

FDA UDI

Class II (US FDA UDI)

by Sirona Dental, Inc.

Identity

Trade Name
XIOS FDA UDI
Generic Name
Dental x-ray film holder, reusable FDA UDI
Device Name
SIRONA HOLDER STARTER KIT S1 SHEATH FDA UDI
Model / Reference
6173632 FDA UDI
Description
SIRONA HOLDER STARTER KIT S1 SHEATH FDA UDI

Identifiers

Primary DI / UDI-DI
D76461736321 FDA UDI
510(k) Number
K933455 FDA UDI
FDA Product Code
EAP FDA UDI
GMDN Term
Dental x-ray film holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1810 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental x-ray film holder, reusable

Xios by Sirona Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film holder, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sirona Dental, Inc.

Sources (1)

  • FDA UDI cf9a31fa-c175-4bc4-8f15-3d834e4356c6 35 fields · synced May 30, 2026