Beautifil Flow Plus X - BEAUTIFIL FLOW PLUS X F03B2 - SHOFU DENTAL CORPORATION

Duns Number:054618202

Device Description: BEAUTIFIL FLOW PLUS X F03B2

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More Product Details

Catalog Number

YN2327

Brand Name

Beautifil Flow Plus X

Version/Model Number

YN2327

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K172530

Product Code Details

Product Code

EBF

Product Code Name

MATERIAL, TOOTH SHADE, RESIN

Device Record Status

Public Device Record Key

5eee6a32-73e7-4ba2-b2a3-18db9cdca12c

Public Version Date

October 15, 2018

Public Version Number

1

DI Record Publish Date

September 14, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SHOFU DENTAL CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 691
2 A medical device with a moderate to high risk that requires special controls. 2950