Perioscopy

GUDID 00840481135262

Perioscopy Explorer, Right, Right

Zest Anchors, LLC

Dental surgical probe, reusable

• Primary Device ID: 00840481135262
• NIH Device Record Key: 916f7d5b-a778-4bc2-9600-257d8970a986
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Perioscopy
• Version Model Number: 1024
• Company DUNS: 078387192
• Company Name: Zest Anchors, LLC
• 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: false
• 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

Customer Support Contacts

• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com
• Phone: +1 877-443-4775
• Email: quality@zestdent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840481135262 [Primary]

FDA Product Code

• EKB: Explorer, Operative

Sterilization

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

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

[00840481135262]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-06
• Device Publish Date: 2024-10-29

On-Brand Devices [Perioscopy]

• 00840481135279: Perioscopy Explorer, Left, Left
• 00840481135262: Perioscopy Explorer, Right, Right
• 00840481135255: Perioscopy Explorer Right
• 00840481135248: Perioscopy Explorer Left