Force DFX Suture-Xtreme™ DFX0034S

GUDID 00850052601188

Force DFX Suture-Xtreme™

DUNAMIS MEDICAL, LLC

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 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 ID00850052601188
NIH Device Record Key28914bba-6d30-42e5-9327-2eb16fd2370b
Commercial Distribution StatusIn Commercial Distribution
Brand NameForce DFX Suture-Xtreme™
Version Model NumberDFX0034S
Catalog NumberDFX0034S
Company DUNS079471560
Company NameDUNAMIS 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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850052601188 [Primary]

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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-08
Device Publish Date2024-01-31

Devices Manufactured by DUNAMIS MEDICAL, LLC

00850052601072 - Hallux Guide2024-06-18 Hallux Guide
00850052601089 - CMC Spacer2024-06-18 CMC Spacer
00850052601096 - CMC Guide2024-06-18 CMC Guide
00850052601157 - Threaded Driver 2024-06-18 Threaded Driver
00850052601232 - Micro Constrictor® Implantation Kit 2024-06-18 Micro Constrictor® Implantation Kit
00850052601225 - Orca Xtreme ™ Kit Knotless Button2024-03-22 Orca Xtreme™ Kit Knotless Button
00850052601188 - Force DFX Suture-Xtreme™2024-02-08Force DFX Suture-Xtreme™
00850052601188 - Force DFX Suture-Xtreme™2024-02-08 Force DFX Suture-Xtreme™
00850052601195 - Fixation Button-Oblong2024-02-08 Fixation Button-Oblong

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.