Nano fx® FURS-0100

GUDID M528FURS01000

NanoFx, Thumble

ARTHROSURFACE INCORPORATED

Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use Subchondral bone needling device lever, single-use
Primary Device IDM528FURS01000
NIH Device Record Key64885158-4901-48f7-bc9b-4d4ce0b31b7c
Commercial Distribution StatusIn Commercial Distribution
Brand NameNano fx®
Version Model NumberFURS-0100
Catalog NumberFURS-0100
Company DUNS144666109
Company NameARTHROSURFACE INCORPORATED
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 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

Customer Support Contacts

Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com
Phone508-520-3003
Emailcontact@arthrosurface.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM528FURS01000 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-04-07
Device Publish Date2015-10-20

Devices Manufactured by ARTHROSURFACE INCORPORATED

M5289V0001000 - KISSloc®2023-09-18 KISSloc, Suture Construct
M5289V0002000 - KISSloc®2023-09-18 KISSloc, Arrow, I K
M52890700013W0 - HemiCAP®2022-02-21 Taper Post, 7.0mm Dia X 13mm Lg, MTP CE
M52890800016A0 - HemiCAP®2022-02-21 8.0mm x 16mm, Taper Post, MTP
M52890800016W0 - HemiCAP®2022-02-21 8.0mm x 16mm, Taper Post, MTP CE
M52890950018A0 - HemiCAP®2022-02-21 9.5mm x 18mm, Taper Post, MTP
M52890950018W0 - HemiCAP®2022-02-21 9.5mm x 18mm, Taper Post, MTP CE
M52891221015A0 - HemiCAP®2022-02-21 12mm Art Comp 1.0mm x 1.5mm, MTP

Trademark Results [Nano fx]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NANO FX
NANO FX
97079610 not registered Live/Pending
ORNUA Co-operative Limited
2021-10-18
NANO FX
NANO FX
85588572 4339832 Live/Registered
ARTHROSURFACE INCORPORATED
2012-04-04
NANO FX
NANO FX
85544880 4377300 Live/Registered
ARTHROSURFACE INCORPORATED
2012-02-16

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