Periodontal Knife

GUDID 00192896102569

Goldman-Fox Periodontal Knife #8 Double Ended "Spear" Offset Blades

SONTEC INSTRUMENTS, INC.

Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife
Primary Device ID00192896102569
NIH Device Record Key7909b8cb-f188-42ce-88d2-4859f94f3fac
Commercial Distribution StatusIn Commercial Distribution
Brand NamePeriodontal Knife
Version Model Number1102-KGF8
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]
GS100192896102569 [Primary]

FDA Product Code

EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL
EMFKNIFE, SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

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