OptimalAkin 6100.5001.04

GUDID 00810136430929

MIS Akin Targeting Instrument, K-wire Cartridge, Left

Forma Medical, Inc.

Orthopaedic prosthesis implantation positioning instrument, single-use

• Primary Device ID: 00810136430929
• NIH Device Record Key: b3d42fda-6f44-4af9-89b7-48726c9e873c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OptimalAkin
• Version Model Number: 6100.5001.04
• Catalog Number: 6100.5001.04
• Company DUNS: 126585966
• Company Name: Forma Medical, Inc.
• 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

Customer Support Contacts

• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com
• Phone: 0000000000
• Email: support@formamedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810136430929 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230945

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

[00810136430929]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-27
• Device Publish Date: 2024-03-19

On-Brand Devices [OptimalAkin]

• 00810136430936: MIS Akin Targeting Instrument, K-wire Cartridge, Right
• 00810136430929: MIS Akin Targeting Instrument, K-wire Cartridge, Left