EZ SPRAY

GUDID 04589551392063

NAKANISHI INC.

Surgical instrument maintenance lubricant

• Primary Device ID: 04589551392063
• NIH Device Record Key: a4de1876-39a0-49e8-aea4-82cdfecae8c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZ SPRAY
• Version Model Number: EZ SPRAY
• Company DUNS: 690710546
• Company Name: NAKANISHI 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: false
• Lot Batch: false
• Serial Number: true
• 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	04589551392063 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163483

FDA Product Code

• EFB: Handpiece, air-powered, dental

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: 2024-11-11
• Device Publish Date: 2024-11-01

Devices Manufactured by NAKANISHI INC.

• 04589551393367 - PANA SPRAY Plus: 2025-10-02
• 04560264576940 - SG20M: 2025-09-05
• 04560264576957 - X-SG20ML: 2025-09-05
• 04589551381500 - NLZ: 2025-09-03
• 04589551381517 - NLZ: 2025-09-03
• 04589551381531 - NLZ: 2025-09-03
• 04589551381562 - NLZ: 2025-09-03
• 04589551381586 - NLZ: 2025-09-03