Solid ePTFE Nasal L Implant ES-L5850

GUDID M724ESL58501

Solid ePTFE Nasal L Implant

IMPLANTECH ASSOCIATES, INC.

Nasal cartilage support implant, non-bioabsorbable
Primary Device IDM724ESL58501
NIH Device Record Keyd01d5604-8336-4e84-9183-4347e8fd976a
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolid ePTFE Nasal L Implant
Version Model Numbersize:5850
Catalog NumberES-L5850
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 Datetrue
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
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
HIBCCM724ESL58501 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FZEProsthesis, Nose, Internal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-11
Device Publish Date2024-11-01

On-Brand Devices [Solid ePTFE Nasal L Implant]

M724ESL62601Solid ePTFE Nasal L Implant
M724ESL58501Solid ePTFE Nasal L Implant

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