Regatta

Variable Angle Screw, 6.0mm Dia. x 35mm

Registry build 21.09.26
14manufacturers in China registered for this device type
40catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for Regatta
Listed by Seaspine Orthopedics Corporation, United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K200885
Record published 2021-02-02
Record revised 2025-10-24 (version 5)

Specifications

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

Catalogue Numbers

Catalogue numbers for Regatta
Catalogue number Size Status
RP3-209010 In distribution
RP1-100418 In distribution
RP1-000210 In distribution
RP1-106035 In distribution
RP3-209100 In distribution
RP1-000212 In distribution
RP1-000220 In distribution
RP1-100416 In distribution
RP1-106060 In distribution
RP1-105560 In distribution
RP3-209020 In distribution
RP1-106065 In distribution
RP1-100412 In distribution
RP1-106040 In distribution
RP1-100414 In distribution
RP1-100218 In distribution
RP1-106045 In distribution
RP1-100220 In distribution
RP1-100408 In distribution
RP1-000218 In distribution
RP1-105540 In distribution
RP3-209001 In distribution
RP1-105535 In distribution
RP1-000216 In distribution
RP1-100216 In distribution
RP1-100212 In distribution
RP1-100210 In distribution
RP1-100410 In distribution
RP3-209200 In distribution
RP1-100214 In distribution
RP1-105545 In distribution
RP1-106055 In distribution
RP2-001000 In distribution
RP1-105550 In distribution
RP1-105565 In distribution
RP1-100208 In distribution
RP1-000208 In distribution
RP1-100420 In distribution
RP1-000214 In distribution
RP1-106050 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212139 2021-09-01
K211903 2021-08-30
K202064 2020-08-26
K200885 2020-05-28
K173521 2018-01-24

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