EXPERIENCE® - EXP C ACO, L 4/5M 022 UL 7-7 FEM 3,4,5HK - Gc Orthodontics America Inc.

Duns Number:063167128

Device Description: EXP C ACO, L 4/5M 022 UL 7-7 FEM 3,4,5HK

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More Product Details

Catalog Number

11/20-2AA5-0168

Brand Name

EXPERIENCE®

Version/Model Number

11/20-2AA5-0168

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

Yes

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

-

Product Code Details

Product Code

EJF

Product Code Name

BRACKET, METAL, ORTHODONTIC

Device Record Status

Public Device Record Key

04fe02e4-dbe4-422c-ab03-dc1dd7d45472

Public Version Date

November 16, 2021

Public Version Number

1

DI Record Publish Date

November 08, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"GC ORTHODONTICS AMERICA INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1781
2 A medical device with a moderate to high risk that requires special controls. 215