Pillar SA Ti

37MM X 28MM AND 40MM X 32MM Hyperlordotic Pillar SA TI Trial Caddy

Registry build 21.09.26
14manufacturers in China registered for this device type
150catalogue numbers in this listing
1510(k) clearance
4recalls 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 Pillar SA Ti
Listed by Orthofix US LLC, 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, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K240749
Record published 2026-07-17

Specifications

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

Catalogue Numbers

Catalogue numbers for Pillar SA Ti
Catalogue number Size Status
82-5535 In distribution
82-9304 In distribution
82-9302 In distribution
82-1220 In distribution
82-3306SP In distribution
82-4010SP In distribution
82-4003SP In distribution
82-3351SP In distribution
82-3358SP In distribution
82-9400 In distribution
82-4404SP In distribution
82-4013SP In distribution
82-3300SP In distribution
82-3312SP In distribution
82-3319SP In distribution
82-3360SP In distribution
82-3350SP In distribution
82-4408SP In distribution
82-3754SP In distribution
82-3321SP In distribution
82-3703SP In distribution
82-9200B In distribution
82-3322SP In distribution
82-3320SP In distribution
82-1218 In distribution
82-1100 In distribution
82-3369SP In distribution
82-3706SP In distribution
82-3308SP In distribution
82-1120 In distribution
82-3311SP In distribution
82-3304SP In distribution
82-3755SP In distribution
82-3718SP In distribution
82-3764SP In distribution
82-3357SP In distribution
82-5035 In distribution
82-3710SP In distribution
82-4407SP In distribution
82-9400B In distribution
82-9300 In distribution
82-3761SP In distribution
82-4402SP In distribution
82-4405SP In distribution
82-3712SP In distribution
82-4008SP In distribution
82-4412SP In distribution
82-9121 In distribution
82-3760SP In distribution
82-9221 In distribution
82-3323SP In distribution
82-3359SP In distribution
82-9100B In distribution
82-4410SP In distribution
82-3305SP In distribution
82-3355SP In distribution
82-3310SP In distribution
82-3714SP In distribution
82-3717SP In distribution
82-9200 In distribution
82-3752SP In distribution
82-3315SP In distribution
82-4017SP In distribution
82-3719SP In distribution
82-3765SP In distribution
82-4406SP In distribution
82-3318SP In distribution
82-3759SP In distribution
82-3766SP In distribution
82-4000SP In distribution
82-9101 In distribution
82-3353SP In distribution
82-9100 In distribution
82-5530 In distribution
82-3700SP In distribution
82-9211 In distribution
82-9303 In distribution
82-3758SP In distribution
82-1150 In distribution
82-9210 In distribution
82-3757SP In distribution
82-3364SP In distribution
82-4012SP In distribution
82-3763SP In distribution
82-3756SP In distribution
82-3753SP In distribution
82-3303SP In distribution
82-5520 In distribution
82-3363SP In distribution
82-4002SP In distribution
82-9305 In distribution
82-9301 In distribution
82-4414SP In distribution
82-3356SP In distribution
82-3366SP In distribution
82-4411SP In distribution
82-3708SP In distribution
82-4400SP In distribution
82-4401SP In distribution
82-3362SP In distribution
82-3309SP In distribution
82-5525 In distribution
82-3711SP In distribution
82-4009SP In distribution
82-3767SP In distribution
82-3301SP In distribution
82-3704SP In distribution
82-1214 In distribution
82-3314SP In distribution
82-3307SP In distribution
82-4001SP In distribution
82-3762SP In distribution
82-1216 In distribution
82-4015SP In distribution
82-3352SP In distribution
82-3715SP In distribution
82-3720SP In distribution
82-3701SP In distribution
82-4005SP In distribution
82-5025 In distribution
82-3354SP In distribution
82-4415SP In distribution
82-3709SP In distribution
82-4014SP In distribution
82-3361SP In distribution
82-4006SP In distribution
82-4004SP In distribution
82-4011SP In distribution
82-3365SP In distribution
82-3702SP In distribution
82-3750SP In distribution
82-9220 In distribution
82-3367SP In distribution
82-9300B In distribution
82-9212 In distribution
82-3716SP In distribution
82-9120 In distribution
82-4413SP In distribution
82-3705SP In distribution
82-3316SP In distribution
82-3317SP In distribution
82-3751SP In distribution
82-3324SP In distribution
82-3302SP In distribution
82-3368SP In distribution
82-4016SP In distribution
82-4416SP In distribution
82-1210 In distribution
82-4403SP In distribution
82-1212 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
K213951 2022-01-05

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Pillar SA Ti
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Orthofix US LLC 510(k) number 2025-06-24 Class II Labeling design A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct. 3
Orthofix US LLC 510(k) number 2025-02-20 Class II Labeling Change Control The product is mislabeled with the incorrect anterior height of 10mm, but the laser marking on the implant and corresponding trial both show the correct anterior height of 10.5mm. 20

Recalls

2 of these are Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2025-11-03 Class III Device Design Labeling contains claims that are not consistently present. 34582
2025-11-03 Class III Device Design Labeling contains claims that are not consistently present. 14201

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