ForceBraid™

GUDID 10818614020768

VALERIS MEDICAL LLC

Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament
Primary Device ID10818614020768
NIH Device Record Key7b743b11-ae50-452a-96f6-a52bc081d60b
Commercial Distribution StatusIn Commercial Distribution
Brand NameForceBraid™
Version Model NumberVAL2024WT
Company DUNS079444554
Company NameVALERIS MEDICAL 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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100818614020761 [Primary]
GS110818614020768 [Package]
Contains: 00818614020761
Package: Box [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GATSuture, Nonabsorbable, Synthetic, Polyethylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-07
Device Publish Date2017-08-17

On-Brand Devices [ForceBraid™]

10818614021222VAL2020WGT
10818614020768VAL2024WT
10818614020751VAL2024BT
10818614020744VAL2020WT
10818614020737VAL2020BBT
10818614020720VAL2016WT
10818614020713VAL2016BT
10818614020690VAL2030WT
10818614020683VAL2030BT
10818614020096VAL0236GL
B048VAL2030WT0ForceBraid™ Suture Tape White
B048VAL2030BT0ForceBraid™ Suture Tape Blue
B048VAL2024WT101
B048VAL2024BT101
VAL2020WT101
B048VAL2020BT1ForceBraid™ Suture Tape, Blue, 20"
B048VAL2016WT1ForceBraid™ Suture Tape, White, 16"
B048VAL2016BT0ForceBraid™ Suture Tape, Blue, 16"
B048VAL0236GL0ForceBraid™ Suture with Loop

Trademark Results [ForceBraid]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FORCEBRAID
FORCEBRAID
86250033 4718004 Live/Registered
ABC Acromion, LLC
2014-04-11

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