← Back to catalogue

XLinearVision

FDA UDI

Class I (US FDA UDI)

by Shenzhen Xpectvision Technology Co., Ltd.

Identity

Trade Name
XLinearVision FDA UDI
Generic Name
Dental x-ray film holder, reusable FDA UDI
Model / Reference
XVH001 FDA UDI

Identifiers

Primary DI / UDI-DI
06972259248035 FDA UDI
FDA Product Code
EGZ FDA UDI
GMDN Term
Dental x-ray film holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.1905 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental x-ray film holder, reusable

XLinearVision by Shenzhen Xpectvision Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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 c921a6b2-f77b-4476-a310-9ab05daf4db5 32 fields · synced Jun 1, 2026