Primary Device ID | 03760225712931 |
NIH Device Record Key | b777c2f0-c8a6-46f9-bd7a-2680edfc91af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEOFIT |
Version Model Number | P10 ST150 |
Catalog Number | P10 ST150 |
Company DUNS | 263616749 |
Company Name | IN2BONES |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760225712931 [Primary] |
HRS | Plate, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
03760225716144 | P01 00381 |
03760225716519 | NEOFIT REVERSIBLE DRILL GUIDE OBLONG HOLES |
03760225716502 | NEOFIT DRILL GUIDE WITH MEASURING FUNCTION |
03760225716168 | HOLDER NEOFIT DRILL GUIDE |
03760225716151 | NEOFIT TRIAL PLATE SIZE 35 MM |
03760225714515 | NEOFIT MTP PLATE LEFT STERILE SIZE 0 - 35 MM |
03760225714508 | NEOFIT MTP PLATE RIGHT STERILE SIZE 0 - 35 MM |
03760225714201 | NEOFIT PLATE BENDER RIGHT |
03760225714195 | NEOFIT PLATE BENDER LEFT |
03760225714188 | NEOFIT MODULAR DRILL GUIDE STD DIAM 2.0 MM |
03760225714171 | NEOFIT DRILL GUIDE OBLONG - LEFT |
03760225714164 | NEOFIT DRILL GUIDE OBLONG - RIGHT |
03760225714157 | NEOFIT DRILL GUIDE STD DIAM 2.0 MM |
03760225714140 | NEOFIT TRIAL PLATE SIZE 50 MM |
03760225714133 | NEOFIT TRIAL PLATE SIZE 45 MM |
03760225714126 | NEOFIT TRIAL PLATE SIZE 40 MM |
03760225714072 | NEOFIT CONTAINER |
03760225713198 | NEOFIT BURRS KIT |
03760225712962 | NEOFIT MTP PLATE LEFT STERILE SIZE 3 - 50 MM |
03760225712955 | NEOFIT MTP PLATE LEFT STERILE SIZE 2 - 45 MM |
03760225712948 | NEOFIT MTP PLATE LEFT STERILE SIZE 1 - 40 MM |
03760225712931 | NEOFIT MTP PLATE RIGHT STERILE SIZE 3- 50 MM |
03760225712924 | NEOFIT MTP PLATE RIGHT STERILE SIZE 2- 45 MM |
03760225712917 | NEOFIT MTP PLATE RIGHT STERILE SIZE 1 - 40 MM |
03701337607227 | NEOFIT BASE CONTAINER |
03701337606077 | NEOFIT PLATE INSTRUMENT POSITION |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEOFIT 97070265 not registered Live/Pending |
Fresh Water Systems, Inc. 2021-10-12 |
NEOFIT 87688194 not registered Live/Pending |
SONDER PRODUCTS PTY LTD 2017-11-16 |
NEOFIT 79319928 not registered Live/Pending |
Kinetic Biosciences Ltd 2021-06-03 |
NEOFIT 79160224 4753979 Live/Registered |
In2Bones 2014-09-04 |
NEOFIT 77978115 3747752 Dead/Cancelled |
DREAMGEAR, LLC 2008-08-14 |
NEOFIT 77902318 3892267 Live/Registered |
Tanner Jeffrey M. 2009-12-29 |
NEOFIT 77546831 not registered Dead/Abandoned |
DREAMGEAR, LLC 2008-08-14 |
NEOFIT 77147392 not registered Dead/Abandoned |
T.R. WORLD GYM- IP, LLC 2007-04-03 |
NEOFIT 77139751 not registered Dead/Abandoned |
Jessup Media 2007-03-25 |
NEOFIT 76354578 3125289 Dead/Cancelled |
CMTLA, Inc. 2002-01-04 |
NEOFIT 75695559 not registered Dead/Abandoned |
Yamane, Alex T. 1999-05-27 |
NEOFIT 74677279 not registered Dead/Abandoned |
Royce Medical Company 1995-05-19 |