LIQUID ETCH LIGHT CURE

GUDID D82813306000

FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC

Orthodontic bracket adhesive

• Primary Device ID: D82813306000
• NIH Device Record Key: a620e3f7-22b5-4ba7-80f1-eafdb58857fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIQUID ETCH LIGHT CURE
• Version Model Number: 1330600
• Company DUNS: 113352686
• Company Name: FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D82813306000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K875143

FDA Product Code

• DYH: Adhesive, Bracket And Tooth Conditioner, Resin

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

Devices Manufactured by FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC

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• D82853004020 - Rickonator: 2024-10-21
• D82851001560 - Bioliner Plus: 2023-02-20
• D82852000920 - Vivos mmRNA: 2021-11-29
• D8281330003 - FUJI SC BAND PASTE PAK: 2018-07-06
• D8281330121 - FUJI LC BAND AUTOMIX: 2018-07-06
• D8281330171 - ULTRA BAND LOK CLEAR: 2018-07-06
• D8281330205 - LIGHT BOND PASTE TIPS: 2018-07-06