Reef L

Reef L is a lateral interbody spacer with a PEEK body, tantalum markers and a one-micron layer of commercially pure titanium called NanoMetalene. The surface has microscopic roughness and…

Registry build 21.09.26

Reef L is a lateral interbody spacer with a PEEK body, tantalum markers and a one-micron layer of commercially pure titanium called NanoMetalene. The surface has microscopic roughness and nanoscale features.

Central windows hold bone graft or a suitable cleared bone-void filler. Footprint, height and lordotic angle vary across the spacer range to accommodate anatomy.

Listed Item

LATERAL IMPLANT, REEF STERILE ASSY 18mm X 10mm X 45mm, 15°

Fixation Configurations

The spacer requires supplemental fixation when used without integrated fixation hardware. TruProfile configurations combine it with a plate, screws and locking covers; a one-hole, single-screw TruProfile construct still requires additional anterior or posterior fixation.

Angle and Supply Scope

For interbody-device use, hyperlordotic sizes greater than 20 degrees require anterior supplemental fixation. Spacers are gamma-sterilized, while the titanium-alloy fixation hardware and associated instruments are supplied nonsterile.

14manufacturers in China registered for this device type
162catalogue numbers in this listing
20510(k) clearances naming this product code
1recall

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 Reef L
Listed by Seaspine Orthopedics Corporation, 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
510(k) K240566
Record published 2024-12-05
Record revised 2025-10-24 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Reef L
Catalogue number Size Status
RL1-104515 In distribution
RL4-185030 In distribution
RL1-224510 In distribution
RL4-383000 In distribution
RL1-224515 In distribution
RL4-265510 In distribution
RL1-264000 In distribution
RL4-145520 In distribution
RL1-225510 In distribution
RL1-285500 In distribution
RL4-166030 In distribution
RL4-322500 In distribution
RL4-124500 In distribution
RL4-104530 In distribution
RL4-383500 In distribution
RL1-225500 In distribution
RL1-124500 In distribution
RL1-125015 In distribution
RL1-204000 In distribution
RL1-125510 In distribution
RL1-126015 In distribution
RL1-264510 In distribution
RL1-226000 In distribution
RL1-285000 In distribution
RL4-244520 In distribution
RL4-245520 In distribution
RL1-185000 In distribution
RL4-164515 In distribution
RL4-284015 In distribution
RL4-224520 In distribution
RL1-164510 In distribution
RL1-244010 In distribution
RL1-145010 In distribution
RL4-246015 In distribution
RL1-164500 In distribution
RL4-245000 In distribution
RL1-245515 In distribution
RL4-184510 In distribution
RL4-224515 In distribution
RL4-165500 In distribution
RL4-165525 In distribution
RL1-205015 In distribution
RL4-145500 In distribution
RL4-244500 In distribution
RL4-206010 In distribution
RL4-245020 In distribution
RL1-224500 In distribution
RL1-164515 In distribution
RL4-244000 In distribution
RL1-244515 In distribution
RL4-204500 In distribution
RL1-106015 In distribution
RL1-184500 In distribution
RL1-124000 In distribution
RL4-284020 In distribution
RL4-265515 In distribution
RL4-244010 In distribution
RL4-144000 In distribution
RL4-323000 In distribution
RL1-286015 In distribution
RL1-205000 In distribution
RL4-125000 In distribution
RL4-363000 In distribution
RL1-204000 In distribution
RL1-224515 In distribution
RL4-184000 In distribution
RL4-124515 In distribution
RL4-224025 In distribution
RL1-145000 In distribution
RL4-264000 In distribution
RL4-104030 In distribution
RL4-224015 In distribution
RL1-245500 In distribution
RL1-284010 In distribution
RL1-205500 In distribution
RL4-304500 In distribution
RL4-245510 In distribution
RL1-225515 In distribution
RL1-125500 In distribution
RL4-126000 In distribution
RL1-266015 In distribution
RL4-225515 In distribution
RL2-100608 In distribution
RL4-186015 In distribution
RL4-266000 In distribution
RL1-204515 In distribution
RL4-266030 In distribution
RL1-185515 In distribution
RL4-165510 In distribution
RL1-164015 In distribution
RL4-265530 In distribution
RL1-145515 In distribution
RL1-145515 In distribution
RL1-165000 In distribution
RL1-166015 In distribution
RL1-284515 In distribution
RL4-265025 In distribution
RL4-266020 In distribution
RL4-184025 In distribution
RL1-185510 In distribution
RL4-146010 In distribution
RL1-165010 In distribution
RL1-284515 In distribution
RL4-125020 In distribution
RL4-165530 In distribution
RL4-166015 In distribution
RL4-106000 In distribution
RL4-364000 In distribution
RL4-285030 In distribution
RL1-144515 In distribution
RL4-284515 In distribution
RL1-184015 In distribution
RL4-105015 In distribution
RL1-224500 In distribution
RL1-264015 In distribution
RL1-124000 In distribution
RL4-204015 In distribution
RL3-109002 In distribution
RL1-144500 In distribution
RL4-284000 In distribution
RL1-226015 In distribution
RL1-126000 In distribution
RL1-284015 In distribution
RL4-166025 In distribution
RL1-105500 In distribution
RL4-285010 In distribution
RL1-104510 In distribution
RL4-265520 In distribution
RL1-144000 In distribution
RL1-125010 In distribution
RL1-144010 In distribution
RL4-225510 In distribution
RL4-164025 In distribution
RL1-184500 In distribution
RL1-146000 In distribution
RL1-226000 In distribution
RL1-126000 In distribution
RL4-144500 In distribution
RL1-225510 In distribution
RL1-205515 In distribution
RL4-244020 In distribution
RL4-184030 In distribution
RL4-166000 In distribution
RL4-105515 In distribution
RL1-204510 In distribution
RL1-205515 In distribution
RL4-185520 In distribution
RL4-125520 In distribution
RL4-224000 In distribution
RL1-145010 In distribution
RL4-264015 In distribution
RL4-124525 In distribution
RL4-165030 In distribution
RL1-186010 In distribution
RL4-125500 In distribution
RL1-145500 In distribution
RL4-205010 In distribution
RL4-286030 In distribution
RL1-106010 In distribution
RL1-204500 In distribution
RL4-144020 In distribution
RL4-124520 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
K253420 2026-07-01
K241466 2024-06-20
K240566 2024-04-26
K233694 2024-01-12
K222732 2022-11-07
K220711 2022-05-10
K213420 2022-05-04
K212540 2021-09-10
K210497 2021-07-07
K210583 2021-06-02
K201755 2020-12-15
K201193 2020-11-25
K200879 2020-06-10
K193636 2020-04-24
K193418 2020-03-13
K192132 2019-12-03
K181079 2018-07-18
K173260 2017-12-04
K173022 2017-10-26
K162715 2016-10-28

Recalls

1 of these is 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
2025-08-06 Class II Device Design Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may r 74

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