SMARTFIT TRY IN HYBRID DENTURE - 3

GUDID 00810126041890

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00810126041890
• NIH Device Record Key: ccbda425-0e7c-4718-9e7a-de6ba94cc205
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SMARTFIT TRY IN HYBRID DENTURE - 3
• Version Model Number: TRYHYD03
• Company DUNS: 796083090
• Company Name: HIOSSEN, 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: true
• Manufacturing Date: true
• 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
GS1	00810126041890 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240688

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2025-04-09
• Device Publish Date: 2025-04-01

Devices Manufactured by HIOSSEN, INC.

• 00810126043245 - ETIII SA (Ø3.2mm) Pre-mounted: 2025-10-07
• 00810126043481 - ET III Fixture NH Regular Pre-Mounted: 2025-10-07
• 00810126043504 - ET III Fixture NH Regular Pre-Mounted: 2025-10-07
• 00810126043511 - ET III Fixture SA Regular Pre-Mounted: 2025-10-07
• 00810126043528 - ET III Fixture NH Regular Pre-Mounted: 2025-10-07
• 00810126043580 - ET III Fixture SA Regular Pre-Mounted: 2025-10-07
• 00810126043597 - ET III Fixture NH Regular Pre-Mounted: 2025-10-07
• 00810126043603 - ET III Fixture SA Regular Pre-Mounted: 2025-10-07