Curvy

GUDID E22120621

VOCO GmbH

Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use Dental wedge, single-use

• Primary Device ID: E22120621
• NIH Device Record Key: 4e340339-b242-4851-af51-3a7e63255cf4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curvy
• Version Model Number: 2062
• Company DUNS: 316699578
• Company Name: VOCO GmbH
• Device Count: 312
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx
• Phone: 999-999-9999
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E2212062 [Unit of Use]
HIBCC	E22120621 [Primary]

FDA Product Code

• KMY: Positioner, Tooth, Preformed

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-13
• Device Publish Date: 2019-05-03

On-Brand Devices [Curvy]

• E22120641: 2064
• E22120631: 2063
• E22120621: 2062
• E22120611: 2061
• E22120601: 2060