Karl Schumacher Composite Putty

GUDID 00842517102163

Regenerative Collagen Dental Bone Graft Composite

KARL SCHUMACHER DENTAL INSTRUMENT CO., INC.

Dental bone matrix implant, synthetic
Primary Device ID00842517102163
NIH Device Record Keyabf37976-faf2-4747-aed0-3c23cca61905
Commercial Distribution StatusIn Commercial Distribution
Brand NameKarl Schumacher Composite Putty
Version Model NumberRCBP0200
Company DUNS043957315
Company NameKARL SCHUMACHER DENTAL INSTRUMENT 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 Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100842517102163 [Primary]

FDA Product Code

LYCBone Grafting Material, Synthetic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-09-26

On-Brand Devices [Karl Schumacher Composite Putty]

00842517102316Regenerative Collagen Dental Bone Graft Composite
00842517102309Regenerative Collagen Dental Bone Graft Composite
00842517102163Regenerative Collagen Dental Bone Graft Composite

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