Lynx Pro 13182

GUDID D950131820

Lynx Pro 550 Handpiece Push button Standard head Non-fiber-optic

LARES RESEARCH

Dental surgical power tool motorized handpiece/set, pneumatic

• Primary Device ID: D950131820
• NIH Device Record Key: a04dfdb6-287d-4374-8971-5a7b94f66bc7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lynx Pro
• Version Model Number: 500 Standard Non-Optic
• Catalog Number: 13182
• Company DUNS: 009127838
• Company Name: LARES RESEARCH
• 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: true
• 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

Customer Support Contacts

• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com
• Phone: 5303451767
• Email: bholderbein@laresdental.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D950131820 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141221

FDA Product Code

• EFB: Handpiece, Air-Powered, Dental

Sterilization

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

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

[D950131820]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-28
• Device Publish Date: 2024-10-18

On-Brand Devices [Lynx Pro]

• D950131840: Lynx Pro 550 Handpiece Push button Mini head 4H Non-Fiber-Optic
• D950131830: Lynx Pro 550 Handpiece Push button Standard Head Fiber Optic
• D950131820: Lynx Pro 550 Handpiece Push button Standard head Non-fiber-optic
• D950131810: Lynx Pro 500 Handpiece Push button Mini head Fiber Optic
• D950131800: Lynx Pro 500 Handpiece Push button Mini head Non-fiber-optic