OASYS (Oral/Nasal Airway System)

GUDID 00810002220210

A removable intraoral device intended to reduce or alleviate snoring and obstructive sleep apnea in adults. This is a reusable device.

JOHN'S DENTAL LABORATORY INC

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• Primary Device ID: 00810002220210
• NIH Device Record Key: 8a54de22-d782-4546-bbe4-9dd82df6a7a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OASYS (Oral/Nasal Airway System)
• Version Model Number: 3014680794
• Company DUNS: 016649253
• Company Name: JOHN'S DENTAL LABORATORY 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: false
• Lot Batch: false
• 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
GS1	00810002220210 [Primary]

FDA Product Code

• LWF: Dilator, Nasal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-05
• Device Publish Date: 2023-03-28