Primary Device ID | 00840420115362 |
NIH Device Record Key | 3115feee-1c09-4d70-aa6e-e98c66c6a6a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G-FORCE |
Version Model Number | 86PS0725 |
Company DUNS | 807201207 |
Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 7 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840420115362 [Primary] |
MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-01 |
00889797058629 | 86PS1000 |
00889797057233 | 86PS1000S |
00840420115393 | 86PS0825 |
00840420115386 | 86PS0510 |
00840420115379 | 86PS0410 |
00840420115362 | 86PS0725 |
00840420115355 | 86PS0615 |
00840420115348 | 86PS0415 |
00840420115331 | 86PS0620 |
00840420115324 | 86PS0515 |
00840420142801 | 86PA50N2 |
00840420142795 | 86PA35N2 |
00840420142771 | 86TA50N2 |
00840420142764 | 86TA35N2 |
00840420142757 | RETIRED |
00889797058711 | 86PS1075 |
00889797058704 | 86PS1065 |
00889797058698 | 86PS1055 |
00889797058681 | 86PS1045 |
00889797058674 | 86PS1008 |
00889797058667 | 86PS1007 |
00889797058650 | 86PS1006 |
00889797058643 | 86PS1005 |
00889797056953 | 86PS1075S |
00889797056946 | 86PS1065S |
00889797056939 | 86PS1055S |
00889797056922 | 86PS1045S |
00889797056915 | 86PS1008S |
00889797056908 | 86PS1007S |
00889797056892 | 86PS1006S |
00889797056885 | 86PS1005S |
00889797042406 | Tenodesis System Hex Driver |
00889797042390 | Tenodesis System Hex Driver |
00889797042321 | Hex Driver |
00889797042291 | Tenodesis System Tendon Scale |
00889797058636 | Drill, Tenodesis System |
00889797058612 | Suture Anchor Pilot Drill Bit |
00889797058605 | Suture Anchor Pilot Drill Bit |
00889797056878 | Tenodesis Drill Bit |
00889797042345 | Tenodesis System Ratcheting Driver Handle |
00889797042284 | Tenodesis System Tissue Protector Handle |
00889797042277 | Tenodesis System Tissue Protector Insert |
00889797042260 | Tenodesis System Tissue Protector Insert |
00889797042253 | Tenodesis System Tissue Protector Insert |
00889797042383 | Tenodesis System Hex Driver |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
G-FORCE 97803428 not registered Live/Pending |
G Force Braces, LLC 2023-02-21 |
G-FORCE 97538230 not registered Live/Pending |
Canid Inc. 2022-08-06 |
G-FORCE 90445279 not registered Live/Pending |
Sunset Capital, LLC 2021-01-01 |
G-FORCE 88935338 not registered Live/Pending |
G-Force Security Enterprises, LLC 2020-05-27 |
G-FORCE 88292254 not registered Live/Pending |
G.P. Reeves Inc. 2019-02-07 |
G-FORCE 87956356 not registered Dead/Abandoned |
G-Force Disc Dog 2018-06-11 |
G-FORCE 87790934 not registered Dead/Abandoned |
VITALITY INNOVATIONS INC. 2018-02-08 |
G-FORCE 87790919 not registered Dead/Abandoned |
VITALITY INNOVATIONS INC. 2018-02-08 |
G-FORCE 87790903 not registered Live/Pending |
VITALITY INNOVATIONS INC. 2018-02-08 |
G-FORCE 87748210 5544670 Live/Registered |
G-FORCE INC. 2018-01-09 |
G-FORCE 87738301 not registered Dead/Abandoned |
GVS Filtration Inc. 2017-12-29 |
G-FORCE 87579201 5428291 Live/Registered |
T-H Marine Supplies, Inc. 2017-08-22 |