Spirotome Spine

The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be used in humans to take out adequate samples of soft tissue from subdermal structures as breast,…

Registry build 21.09.26

The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be used in humans to take out adequate samples of soft tissue from subdermal structures as breast, abdominal wall, thoracic wall, lymph nodes, thyroid, parotis, muscles, and liver. The Spirotome Biopsy Needle Set contains: • A two-part introducer needle that consists of a cutting cannula and a trocar stylet • A helical-tip receiving needle that has been sized to fit through the lumen of the cutting cannula – Injection needle • A release element This presentation has an external diameter of 10G (4 mm) and length of 150 mm.

9manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Zhejiang (4), Jiangsu (3), Guangdong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KNW
Manufacturer City Province Registered as Device types
Zhejiang Curaway Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Plexus (Xiamen) Co., Ltd., Xiamen Fujian Contract manufacturer 3
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Zhejiang Huanyi Sterilization Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 25
Jiana Sterilization Technology (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 23
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4
Suzhou Leapmed Healthcare Corporation Suzhou Jiangsu Contract manufacturer 3

Record

Regulatory record for Spirotome Spine
Listed by Bioncise NV, Belgium
FDA product code KNW
Device type Instrument, Biopsy
Device class Class 2
Regulation 21 CFR 876.1075
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K080095
Record published 2018-08-31
Record revised 2026-04-15 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Spirotome Spine
Catalogue number Size Status
SS10SP In distribution
SS08SP In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Curaway Zhejiang Curaway Medical Technology Co., Ltd. 910
SureAim Coaxial Biopsy Needle Canyon Medical Inc. 157
CorVocet™ Merit Medical Systems, Inc. 157
SureCore Automatic Disposable Biopsy Needle Canyon Medical Inc. 156
M Biopsy Automatic Disposable Biopsy Needle Canyon Medical Inc. 108
M Biopsy Coaxial Biopsy Needle Canyon Medical Inc. 89
Co-Axial Introducer Needle Argon Medical Devices, Inc. 80
SureCore Semi-automatic Disposable Biopsy Needle Canyon Medical Inc. 76
Invivo Philips DS North America LLC 71
Coaxial needle Möller Medical GmbH 68
Disposable needle for reusable biopsy gun Möller Medical GmbH 62
Remington Medical, Inc. Automatic Cutting Needle (NAC) Remington Medical, Inc. 60

Showing 12 of 692. All products under Instrument, Biopsy

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190378 2019-05-24

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Spirotome Spine
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Cook Incorporated 510(k) number 2014-09-26 Class II Package design/selection MEDINVENTS, the manufacturer of the Spirotome” Soft-Tissue Biopsy Needle Set distributed by Cook Medical, has initiated a voluntary recall of these products. The recall has
been initiated due to customer complaints that the protective caps
1239 units 2016-02-02

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