SeaSpine Spacer System – Redondo™

Redondo Implant, 30mm x 24mm x 14mm, 15 Deg Lordotic

Registry build 21.09.26
14manufacturers in China registered for this device type
90catalogue 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 SeaSpine Spacer System – Redondo™
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) K082310
Record published 2015-09-24
Record revised 2025-10-24 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2016-09-02

Catalogue Numbers

Catalogue numbers for SeaSpine Spacer System – Redondo™
Catalogue number Size Status
36-2622 26mm x 24mm x 22mm, 5° In distribution
93-6422 38mm x 26mm x 22mm, 8° In distribution
36-3820 38mm x 26mm x 20mm, 8° In distribution
93-6276 34mm x 24mm x 12mm, 12° In distribution
93-6131 30mm x 24mm x 22mm In distribution
93-6612 26mm x 24mm x 12mm, 8° In distribution
93-6436 38mm x 26mm x 22mm, 12° In distribution
93-6223 30mm x 24mm x 20mm, 10° In distribution
36-3410 34mm x 24mm x 10mm, 8° In distribution
36-3010 30mm x 24mm x 10mm, 5° In distribution
36-3814 38mm x 26mm x 14mm, 8° In distribution
93-6380 30mm x 24mm x 10mm, 5° In distribution
93-6620 26mm x 24mm x 20mm, 8° In distribution
36-3420 34mm x 24mm x 20mm, 8° In distribution
93-6056 30mm x 24mm x 16mm In distribution
93-6384 30mm x 24mm x 14mm, 5° In distribution
36-3016 30mm x 24mm x 16mm, 5° In distribution
93-6232 34mm x 24mm x 12mm, 8° In distribution
93-6060 30mm x 24mm x 20mm In distribution
36-3512 34mm x 24mm x 12mm, 12° In distribution
93-6284 34mm x 24mm x 20mm, 12° In distribution
36-3022 30mm x 24mm x 22mm, 5° In distribution
93-6264 38mm x 26mm x 14mm, 12° In distribution
93-6610 26mm x 24mm x 10mm, 8° In distribution
93-6432 38mm x 26mm x 18mm, 12° In distribution
93-6388 30mm x 24mm x 18mm, 5° In distribution
93-6016 30mm x 24mm x 16mm In distribution
93-6262 38mm x 26mm x 12mm, 12° In distribution
93-6126 30mm x 24mm x 17mm In distribution
93-6020 30mm x 24mm x 10mm In distribution
93-6012 30mm x 24mm x 12mm In distribution
93-6282 34mm x 24mm x 18mm, 12° In distribution
93-6222 30mm x 24mm x 18mm, 10° In distribution
93-6245 34mm x 24mm x 10mm, 12° In distribution
93-6221 30mm x 24mm x 16mm, 10° In distribution
93-6128 30mm x 24mm x 19mm In distribution
93-6418 38mm x 26mm x 18mm, 8° In distribution
36-3916 38mm x 26mm x 16mm, 12° In distribution
36-2612 26mm x 24mm x 12mm, 5° In distribution
36-1514 30mm x 24mm x 14mm, 15° In distribution
93-6241 34mm x 24mm x 16mm, 8° In distribution
93-6382 30mm x 24mm x 12mm, 5° In distribution
36-2614 26mm x 24mm x 14mm, 5° In distribution
93-6260 38mm x 26mm x 10mm, 12° In distribution
93-6050 30mm x 24mm x 10mm In distribution
93-6058 30mm x 24mm x 18mm In distribution
93-6227 30mm x 24mm x 16mm, 15° In distribution
93-6125 30mm x 24mm x 16mm In distribution
93-6274 34mm x 24mm x 10mm, 12° In distribution
93-6412 38mm x 26mm x 12mm, 8° In distribution
93-6410 38mm x 26mm x 10mm, 8° In distribution
93-6129 30mm x 24mm x 20mm In distribution
36-3822 38mm x 26mm x 22mm, 8° In distribution
36-3416 34mm x 24mm x 16mm, 8° In distribution
93-6253 34mm x 24mm x 18mm, 12° In distribution
93-6244 34mm x 24mm x 22mm, 8° In distribution
93-6120 30mm x 24mm x 11mm In distribution
93-6255 34mm x 24mm x 22mm, 12° In distribution
93-6231 34mm x 24mm x 10mm, 8° In distribution
36-1512 30mm x 24mm x 12mm, 15° In distribution
93-6018 30mm x 24mm x 18mm In distribution
93-6272 34mm x 24mm x 22mm, 8° In distribution
93-6268 34mm x 24mm x 18mm, 8° In distribution
93-6110 30mm x 24mm x 10mm In distribution
36-1018 30mm x 24mm x 18mm, 10° In distribution
93-6242 34mm x 24mm x 18mm, 8° In distribution
36-3012 30mm x 24mm x 12mm, 5° In distribution
93-6392 30mm x 24mm x 22mm, 5° In distribution
93-6220 30mm x 24mm x 14mm, 10° In distribution
93-6414 38mm x 26mm x 14mm, 8° In distribution
93-6434 38mm x 26mm x 20mm, 12° In distribution
93-6420 38mm x 26mm x 20mm, 8° In distribution
36-3516 34mm x 24mm x 16mm, 12° In distribution
36-2818 26mm x 24mm x 18mm, 8° Withdrawn
36-4210 30mm x 24mm x 10mm, 12° Withdrawn
36-4822 30mm x 24mm x 22mm, 8° Withdrawn
36-4816 30mm x 24mm x 16mm, 8° Withdrawn
36-4810 30mm x 24mm x 10mm, 8° Withdrawn
36-2822 26mm x 24mm x 22mm, 8° Withdrawn
36-4814 30mm x 24mm x 14mm, 8° Withdrawn
36-2212 26mm x 24mm x 12mm, 12° Withdrawn
36-4818 30mm x 24mm x 18mm, 8° Withdrawn
36-2222 26mm x 24mm x 22mm, 12° Withdrawn
36-1020 30mm x 24mm x 20mm, 10° Withdrawn
36-4212 30mm x 24mm x 12mm, 12° Withdrawn
36-2814 26mm x 24mm x 14mm, 8° Withdrawn
36-2812 26mm x 24mm x 12mm, 8° Withdrawn
36-2820 26mm x 24mm x 20mm, 8° Withdrawn
36-4218 30mm x 24mm x 18mm, 12° Withdrawn
36-4216 30mm x 24mm x 16mm, 12° Withdrawn

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