O-Ring Abutment Retainer

GUDID 08806169100801

Dental Implant System / O-Ring Abutment Retainer D5.15mm X L2.0mm

DENTIS CO., LTD.

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08806169100801
• NIH Device Record Key: 9e8292e2-9f22-4978-a589-12b7e693b3c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: O-Ring Abutment Retainer
• Version Model Number: DOR
• Company DUNS: 688204158
• Company Name: DENTIS CO., LTD.
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806169100801 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K073486

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

[08806169100801]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-08-21

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• 08806169155986 - s-Clean SQ-SL Fixture: 2020-05-01 s-Clean SQ-SL Fixture / D4.1mm X L7.5mm
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• 08806169156006 - s-Clean SQ-SL Fixture: 2020-05-01 s-Clean SQ-SL Fixture / D4.1mm X L11.5mm
• 08806169156013 - s-Clean SQ-SL Fixture: 2020-05-01 s-Clean SQ-SL Fixture / D4.1mm X L13.5mm
• 08806169156020 - s-Clean SQ-SL Fixture: 2020-05-01 s-Clean SQ-SL Fixture / D4.4mm X L7.0mm