Atec 0912-12
9G (3.7MM) X 12CM, 12MM Handpiece
9manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code
7recalls on this code
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.
| 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
| Listed by | Hologic, Inc., United States |
|---|---|
| FDA product code | KNW |
| Device type | Instrument, Biopsy |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1075 |
| Establishment | Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K042290 |
| Record published | 2016-07-26 |
| Record revised | 2024-04-11 (version 5) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Packaging | Box of 5 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| ATEC 0912-12 | In distribution |
Same 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
| Clearance | Decision date |
|---|---|
| K262792 | 2026-08-12 |
| K180233 | 2018-04-10 |
| K163052 | 2017-03-29 |
| K150169 | 2015-08-14 |
Recalls Naming This Product
4 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Hologic, Inc. | 510(k) number | 2010-08-11 | Not classified | Packaging | The firm received a customer complaint that the a device labeled as ATEC 0912-12 was actually ATEC 0912-20. | 990 | 2011-04-13 |
| Hologic, Inc. | 510(k) number | 2010-02-01 | Not classified | Employee error | The product is labeled as ATEC0909-12 but it actually contains 0909-20. | 190 | 2010-10-08 |
| Hologic, Inc. | 510(k) number | 2008-09-22 | Not classified | Process control | The distal tip of the needle may become detached and remain in the patient, requiring surgical removal. | 5,120 (1,024 cases of 5) | 2009-11-18 |
| Suros Surgical Systems, Inc. | 510(k) number | 2006-12-15 | Not classified | Other | The handpiece package may have an incorrect part number on the inner package. Error could result in over-penetration of the biopsy needle. | 1249 handpieces | 2007-05-04 |
Recalls
4 of these are 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.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2025-12-15 | Class II | Under Investigation by firm | Presence of particulates in affected devices that can be deposited into breast tissue during use. | 681,870 units | |
| 2025-01-15 | Class II | Process control | Devices presented a condition in which the inner needle separated from the hub and produced a longer throw of the inner needle or dislodgement. | 55,335 units | |
| 2023-05-02 | Class II | Device Design | The inner needle of the Sertera device is either detaching or discharging and may cause delay in surgery | 756 units | |
| 2016-08-22 | Class II | Labeling Change Control | Incorrect label on the Sertera Biopsy Kit | 570 units | 2017-02-03 |
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.