Jet Flow Bulk Dentin

GUDID 08806387860136

- Jet Flow Bulk is a low viscosity, visible-light activated, flowable. This low stress flowable material is semi-translucent enabling up to a depth of 3~5mm at a time. - Jet Flow Bulk is packaged in disposable tips and two syringes that include restorative materials. - The shades offered with Jet Flow Bulk are Universal(U), Dentin(D), A1, A2, A3. - Jet Flow Bulk contains bisGMA, UDMA, bisEMA. - The fillers are a combination of ytterbium trifluoride filler with a range of particle sizes from 0.053 to 6.76 microns and silica with a particle size range of 0.04 to 0.452 micro micrometre. The inorganic filler loading is approximately 35.6 vol.% (61.0wt.%). Jet Flow Bulk's models are divided according to color: Jet Flow Bulk Universal, Jet Flow Bulk Dentin, Jet Flow Bulk A1, Jet Flow Bulk A2 and Jet Flow Bulk A3.

Meta Biomed Co., Ltd.

Dental composite resin

• Primary Device ID: 08806387860136
• NIH Device Record Key: 62fd6835-06e1-40c2-a86c-3d6941f45f81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jet Flow Bulk Dentin
• Version Model Number: 6013
• Company DUNS: 688322841
• Company Name: Meta Biomed 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806387860136 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242014

FDA Product Code

• EBF: Material, Tooth Shade, Resin

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: 2024-11-25
• Device Publish Date: 2024-11-16

Devices Manufactured by Meta Biomed Co., Ltd.

• 08806387814603 - MX 02-15: 2025-09-03 MGP, 02 Taper 15, 60 Points, P.71
• 08806387814610 - MX 02-20: 2025-09-03 MGP, 02 Taper 20, 60 Points, P.71
• 08806387814627 - MX 02-25: 2025-09-03 MGP, 02 Taper 25, 60 Points, P.71
• 08806387814634 - MX 02-30: 2025-09-03 MGP, 02 Taper 30, 60 Points, P.71
• 08806387814641 - MX 02-35: 2025-09-03 MGP, 02 Taper 35, 60 Points, P.71
• 08806387814658 - MX 02-40: 2025-09-03 MGP, 02 Taper 40, 60 Points, P.71
• 08806387814665 - MX 04-15: 2025-09-03 MGP, 04 Taper 15, 60 Points, P.71
• 08806387814672 - MX 04-20: 2025-09-03 MGP, 04 Taper 20, 60 Points, P.71