Vector

GUDID 00810005666749

Structurally encoded implant 15mm long, 4.0mm diameter. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe.

NVISION BIOMEDICAL TECHNOLOGIES, INC.

Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID00810005666749
NIH Device Record Key8ab6b5c6-419e-48c6-9982-e8015aaacbb3
Commercial Distribution StatusIn Commercial Distribution
Brand NameVector
Version Model NumberHAM-15-40
Company DUNS047486041
Company NameNVISION BIOMEDICAL TECHNOLOGIES, INC.
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

Customer Support Contacts

Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com
Phone210-545-3713
Emaildiana@nvisionbiomed.com

Device Dimensions

Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter
Outer Diameter4 Millimeter
Length15 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100810005666749 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, Fixation, Bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-01-20
Device Publish Date2019-11-30

On-Brand Devices [Vector]

00810005666763Structurally encoded implant 17mm long, 4.0mm diameter. The Vector Hammertoe Correction System
00810005666756Structurally encoded implant 16mm long, 4.0mm diameter. The Vector Hammertoe Correction System
00810005666749Structurally encoded implant 15mm long, 4.0mm diameter. The Vector Hammertoe Correction System
00810005666732Structurally encoded implant 15mm long, 3.5mm diameter. The Vector Hammertoe Correction System
00810005666725Structurally encoded implant 14mm long, 3.5mm diameter. The Vector Hammertoe Correction System
00810005666718Structurally encoded implant 13mm long, 3.5mm diameter. The Vector Hammertoe Correction System
00810005666787Surgical case lid for instrument case. The Vector Hammertoe Correction System is indicated for
00810005666770Inserter for implants 3.5 - 4.0mm diameter instrument. The Vector Hammertoe Correction System i
00810005666602Implant Sizer, general surgical tool. The Vector Hammertoe Correction System is indicated for t
00810005666596Surgical case for holding instruments. The Vector Hammertoe Correction System is indicated for
00810005666589Drill 4.0mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated
00810005666572Drill 3.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated
00810005666565Cannulated Tap 4.0mm diameter instrument. The Vector Hammertoe Correction System is indicated f
00810005666558Cannulated Tap 3.5mm Diameter instrument. The Vector Hammertoe Correction System is indicated f
008100056665411.1mm K-wire, Instrument. The Vector Hammertoe Correction System is indicated for the fixation
00810005668446Drill 4.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated
0081000566929017mm long, 4.0mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566928316mm long, 4.0mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566927615mm long, 4.0mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566926915mm long, 3.5mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566925214mm long, 3.5mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566924513mm long, 3.5mm diameter encoded Hammertoe Implant (Steam). The Vector Hammertoe Correction Sy
0081000566779113mm long, 3.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566099017mm long, 4.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566098316mm long, 4.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566097615mm long, 4.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566096915mm long, 3.5mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566095214mm long, 3.5mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566094513mm long, 3.5mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566093815mm long, 3.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
0081000566092114mm long, 3.0mm diameter Cannulated Hammertoe Implant. The Vector Hammertoe Correction System
00810005667883Double Trocar K-wire, Instrument. The Vector Hammertoe Correction System is indicated for the f
00810005668972Inserter for implants 3.0mm diameter instrument. The Vector Hammertoe Correction System is indi
00810005668965Cannulated Tap 3.0mm diameter instrument. The Vector Hammertoe Correction System is indicated f
0081000566847712mm long, 3.0mm diameter Cannulated Hammertoe Implant (Steam). The Vector Hammertoe Correction
00810005667579Drill 3.0mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated

Trademark Results [Vector]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VECTOR
VECTOR
98873696 not registered Live/Pending
Brampton Engineering Inc.
2024-11-26
VECTOR
VECTOR
98810151 not registered Live/Pending
RELIANCE FOUNDRY CO. LTD.
2024-10-19
VECTOR
VECTOR
98765497 not registered Live/Pending
Industrial Scientific Corporation
2024-09-23
VECTOR
VECTOR
98570106 not registered Live/Pending
EVE UAM, LLC
2024-05-27
VECTOR
VECTOR
98536306 not registered Live/Pending
Innovasis, Inc.
2024-05-06
VECTOR
VECTOR
98535672 not registered Live/Pending
WK KELLOGG NORTH AMERICA LLC
2024-05-06
VECTOR
VECTOR
98492368 not registered Live/Pending
Valtir, LLC
2024-04-10
VECTOR
VECTOR
98452666 not registered Live/Pending
ABS Capitol LLC
2024-03-15
VECTOR
VECTOR
98172446 not registered Live/Pending
Nava Wiegert
2023-09-09
VECTOR
VECTOR
98138465 not registered Live/Pending
P.Q.L., Inc.
2023-08-17
VECTOR
VECTOR
98077441 not registered Live/Pending
Vector Labs, Inc.
2023-07-10
VECTOR
VECTOR
97899193 not registered Live/Pending
CTB IP, INC.
2023-04-20

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