DEXIS Titanium Sensor Kit

GUDID D090101375650

Dental Imaging Technologies Corporation

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• Primary Device ID: D090101375650
• NIH Device Record Key: fb31e30e-6d0e-4dd5-9f97-06aa93e38b90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DEXIS Titanium Sensor Kit
• Version Model Number: 1.013.7565
• Company DUNS: 800111106
• Company Name: Dental Imaging Technologies Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D090101375650 [Primary]
HIBCC	EKAV101375650 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172918

FDA Product Code

• MUH: System, X-Ray, Extraoral Source, Digital

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-14
• Device Publish Date: 2022-03-04

On-Brand Devices [DEXIS Titanium Sensor Kit]

• D090101452100: 1.014.5210
• D090101452090: 1.014.5209
• D090101452070: 1.014.5207
• D090101375650: 1.013.7565
• D090101329130: 1.013.2913