AccuCirc®

GUDID 20814247020097

AccuCirc® Circumcision Device

CLINICAL INNOVATIONS, LLC

Circumcision clamp, single-use
Primary Device ID20814247020097
NIH Device Record Key3f167290-275a-4e46-816b-41dd07812c25
Commercial Distribution StatusIn Commercial Distribution
Brand NameAccuCirc®
Version Model NumberCIRC-1350
Company DUNS809524291
Company NameCLINICAL INNOVATIONS, LLC
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100814247020093 [Primary]
GS110814247020090 [Package]
Contains: 00814247020093
Package: [5 Units]
In Commercial Distribution
GS120814247020097 [Package]
Contains: 10814247020090
Package: [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HFXClamp, Circumcision

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-01

On-Brand Devices [AccuCirc®]

20814247020097AccuCirc® Circumcision Device
20814247020073AccuCirc® Circumcision Device
20814247020059AccuCirc® Circumcision Device
00814247020031AccuCirc® Circumcision Device

Trademark Results [AccuCirc]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACCUCIRC
ACCUCIRC
88705837 not registered Live/Pending
David Tomlinson, MD
2019-11-25
ACCUCIRC
ACCUCIRC
77101460 3402659 Dead/Cancelled
Clinical Innovations, LLC
2007-02-07

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