900-011 Anatomical Malar II Sizer Set 900-011

GUDID M7249000111

Malar Sizer Set

IMPLANTECH ASSOCIATES, INC.

Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis
Primary Device IDM7249000111
NIH Device Record Key8be1aacd-2c17-4774-9e09-9916d1d07f0b
Commercial Distribution StatusIn Commercial Distribution
Brand Name900-011 Anatomical Malar II Sizer Set
Version Model Number900-011
Catalog Number900-011
Company DUNS784664955
Company NameIMPLANTECH ASSOCIATES, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7249000111 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LZKImplant, Malar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


[M7249000111]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-28
Device Publish Date2021-07-20

Devices Manufactured by IMPLANTECH ASSOCIATES, INC.

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