Biopsy Bracket
Reusable non-sterile single-angle bracket for use with Hitachi Aloka Medical UST-979-3.5, UST-989(D)-3.5, UST-990-5, UST-9114-3.5, UST-9115-5, UST-9119, UST-9123, UST-9126, UST-9127,…
Reusable non-sterile single-angle bracket for use with Hitachi Aloka Medical UST-979-3.5, UST-989(D)-3.5, UST-990-5, UST-9114-3.5, UST-9115-5, UST-9119, UST-9123, UST-9126, UST-9127, UST-9130 transducers
Who Else Makes It
Concentrated in Guangdong (18), Jiangsu (10), Shanghai (3). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jabil Circuit (Shanghai) Ltd. | Shanghai | Shanghai | Contract manufacturer | 31 |
| Ming FAI Industrial (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 17 |
| ATL Technology DG,Ltd. | Dongguan | Guangdong | Contract manufacturer | 14 |
| Xuzhou Yongkang Electronic Science Technology Co., Ltd. | Xuzhou | Jiangsu | Contract manufacturer | 13 |
| Hony Medical Co., Ltd. | Taishan | Guangdong | Contract manufacturer | 10 |
| Xian Friendship Medical Electronics Co., Ltd. | Xi’An | Shaanxi | Contract manufacturer | 10 |
| Taijia Medical Electronics (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 10 |
| Chison Medical Technologies Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 5 |
| Philips Ultrasound (Shanghai) Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 5 |
| Shenzhen Mindray BIO-Medical Electronics Co., Ltd. | Shenzhen | Guangdong | Specification developer | 61 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Edan Instruments, Inc. | Shenzhen | Guangdong | Contract manufacturer | 56 |
Showing 12 of 44. All 44 manufacturers in China registered for Transducer, Ultrasonic, Diagnostic
Record
| Listed by | Civco Medical Instruments Co., Inc., United States |
|---|---|
| FDA product code | ITX |
| Device type | Transducer, Ultrasonic, Diagnostic |
| Device class | Class 2 |
| Regulation | 21 CFR 892.1570 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K093713 |
| Record published | 2017-08-22 |
| Record revised | 2022-06-10 (version 11) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, manufacturing date |
| Storage | Special storage condition: Keep Away from Sunlight; Storage environment temperature 52 to 85 °F |
| Sizes | Length 1.4 to 4.53 in; height 1.2 to 2.43 in; width 1.1 to 2.3 in |
| Distribution end date | 2021-02-05 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 698-017 | Length 2.5 in | In distribution | |
| 668-002 | In distribution | ||
| 680-165 | In distribution | ||
| 614-068 | Height 1.83 in | 5 | In distribution |
| 680-088 | Width 1.1 in | In distribution | |
| 667-154 | Width 1.4 in | In distribution | |
| 680-162 | In distribution | ||
| 680-086 | Height 2.2 in | In distribution | |
| 680-087 | Height 2 in | In distribution | |
| 680-068 | Length 2.9 in | In distribution | |
| 680-090 | Height 2.1 in | In distribution | |
| 667-155 | Height 1.2 in | In distribution | |
| 674-069 | Width 1.4 in | In distribution | |
| 610-888 | Width 1.3 in | In distribution | |
| 8260151 | Height 2 in | In distribution | |
| 657-043 | Height 1.89 in | In distribution | |
| 676-188 | Height 1.25 in | In distribution | |
| 644-076 | Length 3.67 in | In distribution | |
| 10658471 | Length 3.74 in | In distribution | |
| 672-003 | Length 3.4 in | In distribution | |
| 680-126 | Length 2.2 in | In distribution | |
| 644-080 | Height 1.68 in | In distribution | |
| 10044759 | Height 1.91 in | In distribution | |
| 644-078 | Length 2.42 in | In distribution | |
| 676-218 | Length 3.8 in | In distribution | |
| 614-091 | Height 1.73 in | In distribution | |
| 698-016 | Height 1.4 in | In distribution | |
| 614-108 | Height 2.05 in | In distribution | |
| 698-020 | Length 3.4 in | In distribution | |
| 680-122 | Length 3.1 in | In distribution | |
| 644-041 | Width 1.31 in | In distribution | |
| 680-085 | Height 2.1 in | In distribution | |
| 742-429 | Length 3.1 in | In distribution | |
| 10787350 | Length 2.74 in | In distribution | |
| 680-128 | Height 1.96 in | In distribution | |
| 657-058 | In distribution | ||
| 614-070 | Width 1.62 in | 5 | In distribution |
| 680-124 | Length 3.8 in | In distribution | |
| 639-057 | Height 1.3 in | In distribution | |
| 680-177 | In distribution | ||
| 644-083 | Height 2.43 in | In distribution | |
| 680-171 | Length 1.6 in | In distribution | |
| 680-093 | Width 1.2 in | In distribution | |
| 639-056 | Length 2.95 in | In distribution | |
| 7471159 | Height 1.4 in | In distribution | |
| 742-493 | Length 3.3 in | In distribution | |
| 10038223 | Height 1.95 in | In distribution | |
| 680-062 | Length 2.9 in | In distribution | |
| 657-039 | Width 1.69 in | In distribution | |
| 644-074 | Height 2.43 in | In distribution | |
| 7471134 | Length 2.7 in | Withdrawn | |
| 614-063 | Width 1.46 in | Withdrawn | |
| 614-112 | Height 1.96 in | Withdrawn | |
| 742-359-10 | Width 1.4 in | 10 | Withdrawn |
| 698-021 | Length 3.2 in | Withdrawn | |
| 742-429-10 | Height 1.3 in | 10 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| SonoScape | Sonoscape Medical Corp. | 302 |
| Biopsy Starter Kit | Civco Medical Instruments Co., Inc. | 172 |
| Sheathes | Sheathing Technologies, Inc. | 170 |
| Needle Guide | Civco Medical Instruments Co., Inc. | 156 |
| Sheathes3D | Sheathing Technologies, Inc. | 78 |
| Ultrasound Probe Cover Biopsy Needle Guide | Advance Medical Designs, Inc. | 78 |
| ultrasonic transducer | Edan Instruments, Inc. | 70 |
| Unbranded | Advance Medical Designs, Inc. | 68 |
| Reusable Biopsy Bracket | Protek Medical Products, Inc. | 60 |
| Ultrasound Probe Cover Biopsy Needle Guide Kit | Advance Medical Designs, Inc. | 58 |
| Transducer Cover | Civco Medical Instruments Co., Inc. | 54 |
| Needle Guide Starter Kit | Civco Medical Instruments Co., Inc. | 52 |
Showing 12 of 1,678. All products under Transducer, Ultrasonic, Diagnostic
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K231783 | 2023-11-14 |
| K222052 | 2022-11-22 |
| K211270 | 2021-09-13 |
| K163313 | 2017-06-09 |
| K160806 | 2016-08-05 |
| K131161 | 2013-09-17 |
| K131528 | 2013-06-11 |
| K093713 | 2010-01-19 |
| K013721 | 2001-12-28 |
| K992152 | 1999-08-17 |
| K991236 | 1999-06-02 |
| K970513 | 1997-06-20 |
| K970514 | 1997-06-20 |
| K970515 | 1997-06-20 |
| K843573 | 1984-12-13 |
Recalls Naming This Product
10 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 |
|---|---|---|---|---|---|---|---|
| Civco Medical Instruments Co., Inc. | 510(k) number | 2025-05-01 | Class II | Process design | During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place. | 506 boxes | |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2018-07-30 | Class II | Process control | The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. | 107 units | 2020-09-16 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2018-07-30 | Class II | Process control | The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. | 3 units | 2020-09-16 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2018-02-23 | Class II | Device Design | A cover failed leak testing during validation testing of new needle guides from a replacement tool. | 177 boxes | 2020-10-06 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2015-10-21 | Class II | Process design | Sterility of the product cannot be assured. | 717 boxes | 2017-02-28 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2015-10-21 | Class II | Process design | Sterility of the product cannot be assured. | 508 boxes | 2017-02-28 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2015-10-21 | Class II | Process design | Sterility of the product cannot be assured. | 1139 boxes | 2017-02-28 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2015-10-21 | Class II | Process design | Sterility of the product cannot be assured. | 206 boxes | 2017-02-28 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2015-10-21 | Class II | Process design | Sterility of the product cannot be assured. | 54 boxes | 2017-02-28 |
| Civco Medical Instruments Co., Inc. | 510(k) number | 2008-01-16 | Not classified | Packaging | Incorrect Needle Guide- The individual pouches contained V53W Endocavity Needle guide(p/n/034-054) instead of the Shimadzu T/R Needle guide (p/n134-054). | Lot M102250 – 5 boxes; Lot M105440 – 2 boxes | 2008-04-03 |
Recalls
16 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 |
|---|---|---|---|---|---|
| 2018-11-02 | Class II | Other | 613 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 49 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 66 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 20 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 234 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 115 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. | 948 boxes | 2020-11-20 |
| 2018-11-02 | Class II | Other | The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. | 738 boxes | 2020-11-20 |
| 2018-11-02 | Class II | Other | 73 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 257 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 468 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 3 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | 297 boxes | 2020-11-20 | |
| 2018-11-02 | Class II | Other | The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. | 1,375 boxes | 2020-11-20 |
| 2018-11-02 | Class II | Other | 135 boxes | 2020-11-20 | |
| 2015-02-26 | Class II | Process design | Leaks were detected in the recalled lot which may compromise the sterility of the product. | 120 pouches | 2017-02-28 |
| 2011-01-21 | Not classified | Labeling design | Non-sterile transducer covers were incorrectly labeled as sterile and contained incorrect temperature storage information. | 31/24-cover boxes | 2013-07-09 |
| 2010-07-20 | Not classified | Nonconforming Material/Component | Polyethylene material did not have proper treatment applied during manufacturing. Untreated polyethylene material does not maintain a secure seal with the adhesive tape used to secure the tip to the cover. | 22 boxes | 2012-04-13 |
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.