RESINCAP POWDER 2380RED

GUDID D6502380RED0

PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER

LANG DENTAL MANUFACTURING CO., INC.

Temporary dental crown/bridge resin
Primary Device IDD6502380RED0
NIH Device Record Key20225f1d-9203-4999-9e25-68e2cf6b734f
Commercial Distribution StatusIn Commercial Distribution
Brand NameRESINCAP POWDER
Version Model Number45.4 KG
Catalog Number2380RED
Company DUNS005185798
Company NameLANG DENTAL MANUFACTURING CO., INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD6502380RED0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EBGCrown And Bridge, Temporary, Resin

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-10-29
Device Publish Date2016-09-01

On-Brand Devices [RESINCAP POWDER]

D6502390RED0PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER
D6502380RED0PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER
D6502370RED0PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER
D6502350RED0PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER
D6502310RED0PATTERN, COPING AND INLAY ACRYLIC RESIN POWDER

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