ProLift Trial

196 catalogue numbers from 151-459, listed by Life Spine, United States, under Intervertebral Fusion Device With Bone Graft, Lumbar. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
196catalogue numbers in this listing
33510(k) clearances naming this product 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 ProLift Trial
Listed by Life Spine, 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, Manufacturer
510(k) K190488
Record published 2019-11-07
Record revised 2025-07-14 (version 3)

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

Catalogue Numbers

Catalogue numbers for ProLift Trial
Catalogue number Size Status
151-459 In distribution
151-411 In distribution
151-511 In distribution
151-551 In distribution
151-394 In distribution
151-547 In distribution
151-467 In distribution
151-485 In distribution
151-427 In distribution
151-414 In distribution
151-517 In distribution
151-429 In distribution
151-553 In distribution
151-434 In distribution
151-462 In distribution
151-562 In distribution
151-555 In distribution
151-588 In distribution
151-558 In distribution
151-395 In distribution
151-496 In distribution
151-595 In distribution
151-379 In distribution
151-475 In distribution
151-432 In distribution
151-585 In distribution
151-523 In distribution
151-494 In distribution
151-536 In distribution
151-571 In distribution
151-385 In distribution
151-583 In distribution
151-384 In distribution
151-482 In distribution
151-473 In distribution
151-472 In distribution
151-405 In distribution
151-519 In distribution
151-579 In distribution
151-470 In distribution
151-392 In distribution
151-550 In distribution
151-480 In distribution
151-415 In distribution
151-464 In distribution
151-591 In distribution
151-556 In distribution
151-549 In distribution
151-452 In distribution
151-559 In distribution
151-590 In distribution
151-376 In distribution
151-499 In distribution
151-542 In distribution
151-397 In distribution
151-495 In distribution
151-431 In distribution
151-563 In distribution
151-578 In distribution
151-489 In distribution
151-450 In distribution
151-502 In distribution
151-441 In distribution
151-478 In distribution
151-381 In distribution
151-393 In distribution
151-388 In distribution
151-566 In distribution
151-404 In distribution
151-492 In distribution
151-461 In distribution
151-413 In distribution
151-529 In distribution
151-528 In distribution
151-418 In distribution
151-451 In distribution
151-416 In distribution
151-456 In distribution
151-572 In distribution
151-466 In distribution
151-449 In distribution
151-540 In distribution
151-408 In distribution
151-417 In distribution
151-522 In distribution
151-576 In distribution
151-525 In distribution
151-453 In distribution
151-554 In distribution
151-564 In distribution
151-419 In distribution
151-407 In distribution
151-437 In distribution
151-484 In distribution
151-548 In distribution
151-474 In distribution
151-503 In distribution
151-516 In distribution
151-509 In distribution
151-501 In distribution
151-487 In distribution
151-586 In distribution
151-425 In distribution
151-423 In distribution
151-535 In distribution
151-518 In distribution
151-471 In distribution
151-541 In distribution
151-533 In distribution
151-440 In distribution
151-398 In distribution
151-584 In distribution
151-582 In distribution
151-560 In distribution
151-581 In distribution
151-575 In distribution
151-444 In distribution
151-568 In distribution
151-386 In distribution
151-570 In distribution
151-391 In distribution
151-438 In distribution
151-389 In distribution
151-465 In distribution
151-412 In distribution
151-513 In distribution
151-446 In distribution
151-445 In distribution
151-426 In distribution
151-468 In distribution
151-460 In distribution
151-443 In distribution
151-476 In distribution
151-382 In distribution
151-409 In distribution
151-508 In distribution
151-531 In distribution
151-497 In distribution
151-454 In distribution
151-463 In distribution
151-574 In distribution
151-530 In distribution
151-593 In distribution
151-491 In distribution
151-421 In distribution
151-458 In distribution
151-557 In distribution
151-537 In distribution
151-504 In distribution
151-524 In distribution
151-569 In distribution
151-505 In distribution
151-527 In distribution
151-420 In distribution
151-520 In distribution
151-486 In distribution
151-514 In distribution
151-399 In distribution
151-481 In distribution
151-580 In distribution
151-483 In distribution
151-552 In distribution
151-538 In distribution
151-401 In distribution
151-493 In distribution
151-592 In distribution
151-546 In distribution
151-469 In distribution
151-377 In distribution
151-500 In distribution
151-410 In distribution
151-506 In distribution
151-507 In distribution
151-406 In distribution
151-436 In distribution
151-577 In distribution
151-390 In distribution
151-396 In distribution
151-448 In distribution
151-526 In distribution
151-544 In distribution
151-430 In distribution
151-594 In distribution
151-498 In distribution
151-573 In distribution
151-539 In distribution
151-439 In distribution
151-403 In distribution
151-515 In distribution
151-442 In distribution
151-447 In distribution
151-521 In distribution
151-387 In distribution
151-428 In distribution
151-561 In distribution
151-383 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
K261430 2026-07-28
K260837 2026-05-12
K253748 2026-01-23
K251502 2025-07-07
K250373 2025-04-09
K243668 2025-01-23
K242826 2024-10-08
K232611 2023-11-30
K223430 2023-05-04
K221806 2022-12-05
K213417 2022-09-29
K212520 2021-10-08
K210061 2021-04-30
K203361 2021-03-17
K201721 2020-09-04
K201500 2020-08-04
K193521 2020-02-06
K193258 2020-01-31
K190721 2019-11-14
K190488 2019-07-23
K191005 2019-06-13
K181625 2018-12-11
K182470 2018-11-26
K172105 2018-02-02
K173182 2017-12-20
K170919 2017-08-03
K153400 2016-03-07
K133717 2014-09-19
K131077 2013-07-17
K130630 2013-06-13
K121116 2012-05-08
K111569 2011-07-06
K080411 2008-05-15

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