Lucent L

Lucent® L 18MM X 60MM X 11MM 12° Cage, PC

Registry build 21.09.26
14manufacturers in China registered for this device type
168catalogue numbers in this listing
17510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Lucent L
Listed by Spinal Elements, Inc., United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2019-08-02
Record revised 2025-07-21 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Lucent L
Catalogue number Size Status
P11850-608 In distribution
P12265-608A In distribution
P12240-610 In distribution
P12250-610 In distribution
P12240-208 In distribution
P11860-211 In distribution
P12240-209 In distribution
P12245-210 In distribution
P12255-209 In distribution
P12240-812 In distribution
P11845-614 In distribution
P12240-215 In distribution
P12260-616 In distribution
P12245-808 In distribution
P11855-610 In distribution
P11855-215 In distribution
P11860-209 In distribution
P12260-215 In distribution
P12260-209 In distribution
P11840-216 In distribution
P12240-214 In distribution
P12255-810 In distribution
P11860-612 In distribution
P12255-213 In distribution
P12250-209 In distribution
P12255-610 In distribution
P12260-211 In distribution
P11860-208 In distribution
P11850-612 In distribution
P11850-210 In distribution
P12240-808 In distribution
P12240-810 In distribution
P12265-610A In distribution
P12245-208 In distribution
P11850-207 In distribution
P11855-209 In distribution
P12250-608 In distribution
P12260-208 In distribution
P12260-213 In distribution
P12260-212 In distribution
P11845-214 In distribution
P12260-216 In distribution
P12250-614 In distribution
P11855-212 In distribution
P12240-614 In distribution
P11865-608A In distribution
P12260-612 In distribution
P12255-207 In distribution
P11840-210 In distribution
P11845-610 In distribution
P11850-213 In distribution
P12255-614 In distribution
P11850-209 In distribution
P12255-608 In distribution
P11845-608 In distribution
P12245-610 In distribution
P12255-612 In distribution
P12240-211 In distribution
P11850-610 In distribution
P12245-209 In distribution
P12245-214 In distribution
P11840-214 In distribution
P11855-207 In distribution
P12255-808 In distribution
P11840-207 In distribution
P12245-608 In distribution
P11860-215 In distribution
P11845-213 In distribution
P12250-610A In distribution
P11840-211 In distribution
P12245-211 In distribution
P11855-216 In distribution
P11855-612 In distribution
P12255-214 In distribution
P12265-612A In distribution
P12245-612 In distribution
P12245-216 In distribution
P11850-216 In distribution
P12255-812 In distribution
P11850-212 In distribution
P12250-208 In distribution
P12245-810 In distribution
P11855-214 In distribution
P11855-213 In distribution
P11845-612 In distribution
P11855-614 In distribution
P12250-211 In distribution
P12240-216 In distribution
P12245-207 In distribution
P11850-208 In distribution
P12255-208 In distribution
P11865-612A In distribution
P12250-212 In distribution
P12260-614 In distribution
P12245-212 In distribution
P11860-210 In distribution
P12260-614A In distribution
P12260-210 In distribution
P12260-214 In distribution
P12255-210 In distribution
P12250-214 In distribution
P12260-812 In distribution
P11860-214 In distribution
P11840-608 In distribution
P12250-210 In distribution
P12245-213 In distribution
P11850-215 In distribution
P12245-215 In distribution
P11840-212 In distribution
P12260-808 In distribution
P11845-208 In distribution
P12240-212 In distribution
P11850-614 In distribution
P11850-214 In distribution
P12250-612 In distribution
P11840-213 In distribution
P11855-208 In distribution
P12240-213 In distribution
P11860-608 In distribution
P11850-211 In distribution
P11855-608 In distribution
P11840-208 In distribution
P12265-614A In distribution
P12250-812 In distribution
P12255-216 In distribution
P12260-608 In distribution
P11840-610 In distribution
P12240-207 In distribution
P11845-211 In distribution
P11840-614 In distribution
P11860-614 In distribution
P11860-213 In distribution
P11845-207 In distribution
P12260-207 In distribution
P11840-209 In distribution
P12245-614 In distribution
P11860-207 In distribution
P11860-212 In distribution
P11840-612 In distribution
P12255-215 In distribution
P12260-610 In distribution
P11855-210 In distribution
P11860-216 In distribution
P12250-207 In distribution
P12255-211 In distribution
P12250-808 In distribution
P12260-613 In distribution
P12240-612 In distribution
P12245-812 In distribution
P12250-810 In distribution
P11840-215 In distribution
P12255-212 In distribution
P12250-614A In distribution
P12250-216 In distribution
P11865-610A In distribution
P11845-216 In distribution
P12250-215 In distribution
P12240-210 In distribution
P11845-215 In distribution
P12240-608 In distribution
P11865-614A In distribution
P11845-212 In distribution
P11860-610 In distribution
P11855-211 In distribution
P12260-810 In distribution
P11845-209 In distribution
P11845-210 In distribution
P12250-213 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260506 2026-05-15
K250773 2026-02-04
K234150 2024-03-27
K231252 2023-06-30
K210044 2021-06-30
K203254 2021-03-26
K202298 2020-12-22
K182584 2018-12-10
K181837 2018-11-02
K170235 2017-11-29
K152011 2016-06-09
K150061 2015-05-19
K122967 2013-02-21
K110632 2012-05-23
K081968 2008-08-05
K073348 2007-12-26
K071724 2007-11-09

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-04-16 Class II Labeling mix-ups Omega LIF interbody implants labeled as having 11 degrees of lordosis was assembled using components manufactured with 4 degrees of lordosis. 19 units
2014-12-18 Class II Labeling False and Misleading Spinal Elements is recalling the Ti-Bond related brochures that includes LT-10000 and MP-14000 (all revisions) the content regarding the Ti-Bond coating within the literature is unsubstantiated in context and/or misleading for the coating’s 1200 units 2015-03-10

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer