LSA Dental Implants RP LSA-300015

GUDID 07290120486812

SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD

Dental implant system

• Primary Device ID: 07290120486812
• NIH Device Record Key: 90a1b08c-5068-4fda-bd7e-b2907cf06507
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LSA Dental Implants RP
• Version Model Number: 4.3 x 11.5mm
• Catalog Number: LSA-300015
• Company DUNS: 514799902
• Company Name: SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	07290120486812 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242217

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

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: 2026-03-10
• Device Publish Date: 2026-03-02

On-Brand Devices [LSA Dental Implants RP]

• 72901204866713: 4.3 x 8mm
• 07290120487116: 5.0 x 13mm
• 07290120487062: 5.0 x 11.5mm
• 07290120487017: 5.0 x 10mm
• 07290120486966: 5.0 x 8mm
• 07290120486911: 4.3 x 15mm
• 07290120486867: 4.3 x 13mm
• 07290120486812: 4.3 x 11.5mm
• 07290120486768: 4.3 x 10mm