Lucent®

Intervertebral Fusion Device With Bone Graft, Lumbar

Spinal Elements Inc.

The following data is part of a premarket notification filed by Spinal Elements Inc. with the FDA for Lucent®.

Pre-market Notification Details

Device IDK170235
510k NumberK170235
Device Name:Lucent®
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant Spinal Elements Inc. 3115 Melrose Dr., Suite 200 Carlsbad,  CA  92010
ContactJulie Lamothe
CorrespondentJulie Lamothe
Spinal Elements Inc. 3115 Melrose Dr., Suite 200 Carlsbad,  CA  92010
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-01-25
Decision Date2017-11-29

Trademark Results [Lucent]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LUCENT
LUCENT
98363852 not registered Live/Pending
Applied Materials, Inc.
2024-01-18
LUCENT
LUCENT
98362973 not registered Live/Pending
Habby, LLC
2024-01-18
LUCENT
LUCENT
98351345 not registered Live/Pending
Dayah, Michael J.
2024-01-10
LUCENT
LUCENT
98302177 not registered Live/Pending
Kotzeva, Mariana
2023-12-06
LUCENT
LUCENT
97531251 not registered Live/Pending
Ocaso Group LLC
2022-08-02
LUCENT
LUCENT
97359144 not registered Live/Pending
Schneller LLC
2022-04-12
LUCENT
LUCENT
97118936 not registered Live/Pending
Smart, LLC
2021-11-10
LUCENT
LUCENT
90977139 not registered Live/Pending
Lucent Surgical Support Systems, Inc.
2021-05-11
LUCENT
LUCENT
90865531 not registered Live/Pending
Lucent Industry Co., Ltd.
2021-08-04
LUCENT
LUCENT
90703416 not registered Live/Pending
Lucent Surgical Support Systems, Inc.
2021-05-11
LUCENT
LUCENT
90459149 not registered Live/Pending
Swarovski Aktiengesellschaft
2021-01-11
LUCENT
LUCENT
87679949 not registered Dead/Abandoned
Modne, Inc.
2017-11-10

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