Immediate Provisional Implant 29544

GUDID 17332747000693

Immediate Provisional Implant

Nobel Biocare AB

Screw endosteal dental implant, two-piece

• Primary Device ID: 17332747000693
• NIH Device Record Key: bfd503b8-513f-4ec4-9b2b-6773748471d2
• Commercial Distribution Discontinuation: 2018-03-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Immediate Provisional Implant
• Version Model Number: 29544
• Catalog Number: 29544
• Company DUNS: 353939929
• Company Name: Nobel Biocare AB
• Device Count: 1
• DM Exempt: true
• 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: true
• 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: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07332747016451 [Primary]
GS1	17332747000693 [Package]; Contains: 07332747016451; Package: Pack [10 Units]; Discontinued: 2018-03-02; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K984287

FDA Product Code

• DZE: IMPLANT, ENDOSSEOUS, ROOT-FORM

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-05-31
• Device Publish Date: 2015-09-17

Devices Manufactured by Nobel Biocare AB

• 07332747225549 - NobelActive®: 2026-03-10 Guided Implant Mount NobelActive S 4.3
• 07332747225556 - NobelActive®: 2026-03-10 Guided Implant Mount NobelActive S 5.0
• 07332747225563 - NA: 2026-03-10 Guided Implant Mount CC S 4.3
• 07332747225570 - NA: 2026-03-10 Guided Implant Mount CC S 5.0/5.5
• 07332747225587 - NA: 2026-03-10 Guided Templ Abutm w Screw CC S 4.3
• 07332747225594 - NA: 2026-03-10 Guided Templ Abutm w Screw CC S 5.0/5.5
• 07332747225839 - NobelActive®: 2026-03-10 Guided Implant Mount NobelActive S 5.5
• 07332747221947 - NobelActive® S TiUltra™: 2026-03-06 NobelActive® S TiUltra™ NP 3.5x8.5mm