GRYPHON Flex 208960

GUDID 10886705032518

GRYPHON Flex Knotless Anchor Sawtooth Curved Guide

Medos International Sàrl

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable
Primary Device ID10886705032518
NIH Device Record Keyb4d60685-690e-4bff-b361-af141a034192
Commercial Distribution StatusIn Commercial Distribution
Brand NameGRYPHON Flex
Version Model Number208960
Catalog Number208960
Company DUNS482661753
Company NameMedos International Sàrl
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110886705032518 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-27
Device Publish Date2024-05-17

On-Brand Devices [GRYPHON Flex]

10886705032846GRYPHON Flex Knotless Anchor Hard Bone Drill [Disposable]
10886705032532GRYPHON Flex Knotless Anchor Straight Drill
10886705032525GRYPHON Flex Knotless Anchor Sawtooth Straight Guide
10886705032518GRYPHON Flex Knotless Anchor Sawtooth Curved Guide
10886705032501GRYPHON Flex Knotless Anchor Curved Drill [Disposable]
10886705032488GRYPHON Flex Knotless PEEK Anchor PEEK Anchor STRAIGHT
10886705032464GRYPHON Flex Knotless Anchor Obturator
10886705032457GRYPHON Flex Knotless Anchor Fishmouth Straight Guide
10886705032440GRYPHON Flex Knotless Anchor Fishmouth Curved Guide
10886705032433GRYPHON Flex Knotless Biocomposite Anchor TCP/PLLA Anchor STRAIGHT

Trademark Results [GRYPHON Flex]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GRYPHON FLEX
GRYPHON FLEX
90501667 not registered Live/Pending
Johnson & Johnson
2021-02-01

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