Nanice

GUDID 00860007349102

Endoscopic Carpal Tunnel Kit

Nanice Medical Solutions, LLC

Arthroscopic surgical procedure kit, non-medicated, single-use
Primary Device ID00860007349102
NIH Device Record Key89a3cc91-6ddb-420f-880e-043bb536838c
Commercial Distribution StatusIn Commercial Distribution
Brand NameNanice
Version Model NumberAT18-0000
Company DUNS051618557
Company NameNanice Medical Solutions, LLC
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

Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com
Phone2156497666
Emailnanicemedical@gmail.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860007349102 [Primary]

FDA Product Code

NBHAccessories, Arthroscopic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-12-13
Device Publish Date2022-12-22

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