Renova 43009K

GUDID D76843009K0

Sleeve w/screw

KEYSTONE DENTAL, INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: D76843009K0
• NIH Device Record Key: d2f95200-482d-49b8-93fa-c636c479ccb7
• Commercial Distribution Discontinuation: 2019-04-26
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Renova
• Version Model Number: 43009K
• Catalog Number: 43009K
• Company DUNS: 787471015
• Company Name: KEYSTONE DENTAL, INC.
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com
• Phone: +1(866)902-9272
• Email: info@keystonedental.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D76843009K0 [Primary]

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-04-07
• Device Publish Date: 2016-02-04

On-Brand Devices [Renova]

• D76843121K0: Fixed Detach Abutment
• D76843120K0: Fixed Detach Abutment
• D76843119K0: Fixed Detach Abutment
• D76843118K0: Fixed Detach Abutment
• D76843116K0: Abutment Screw
• D76843114K0: UCLA Abutment
• D76843113K0: UCLA Abutment
• D76843111K0: UCLA Abutment
• D76843110K0: UCLA Abutment
• D76843109K0: Snap Abutment
• D76843108K0: Snap Abutment
• D76843107K0: Snap Abutment
• D76843106K0: Snap Abutment
• D76843105K0: Snap Abutment
• D76843104K0: Snap Abutment
• D76843103K0: Snap Abutment
• D76843102K0: Snap Abutment
• D76843100K0: Abutment Screw
• D76843096K0: COC Abutment
• D76843094K0: COC Abutment
• D76843092K0: COC Abutment
• D76843090K0: COC Abutment
• D76843089K0: COC Abutment
• D76843010K0: Sleeve w/screw
• D76843009K0: Sleeve w/screw
• D76843007K0: Sleeve w/screw
• D76843006K0: Sleeve w/screw
• D76810040K0: Healing Abutment
• D76810039K0: Healing Abutment
• D76810038K0: Healing Abutment
• D76810037K0: Healing Abutment
• D76810036K0: Healing Abutment
• D76810035K0: Healing Abutment
• D76810033K0: Cover Screw
• D76810032K0: Cover Screw