INRO Surgical Nail 4R

GUDID 10861887000210

Nail splint for the reconstructive surgery of the nail bed.

Inro Medical Designs Inc

Hand/finger splint, single-use
Primary Device ID10861887000210
NIH Device Record Key641f41c8-2716-415c-b629-5f9ae90109c7
Commercial Distribution StatusIn Commercial Distribution
Brand NameINRO Surgical Nail
Version Model Number00-4R
Catalog Number4R
Company DUNS623674272
Company NameInro Medical Designs 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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com
Phone1 800 527 1093
Emailinfo@inro.com

Device Dimensions

Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter
Width14 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100861887000213 [Primary]
GS110861887000210 [Package]
Contains: 00861887000213
Package: form filled seal [1 Units]
Discontinued: 2024-12-31
In Commercial Distribution

FDA Product Code

FYHSplint, Extremity, Noninflatable, External, Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-25
Device Publish Date2023-08-17

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.