HSG Tray
For hysterosalpingography procedures
40manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
4recalls on this code
Who Else Makes It
Concentrated in Jiangsu (15), Zhejiang (15), Shanghai (5). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hangzhou Rollmed Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 127 |
| Amsino Medical (Kunshan) Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 53 |
| Conod Medical Co., Limited | Changshu | Jiangsu | Contract manufacturer | 48 |
| Hangzhou Fushan Medical Appliance Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 44 |
| Linhai Deyi Plastic Co., Ltd. | Linhai | Zhejiang | Contract manufacturer | 15 |
| Shenzhen HYS Medical Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 6 |
| Boen Healthcare Co., Ltd. | Suzhou | Jiangsu | Specification developer | 263 |
| Hospital & Homecare IMP. & EXP. Co., Ltd. | Nanjing | Jiangsu | Contract manufacturer | 179 |
| Jiangsu NEW Pentastar Medical Products Co., Ltd. | Changzhou | Jiangsu | Exporter | 146 |
| Huzhou Junda Industry Co., Ltd. | Anji | Zhejiang | Contract manufacturer | 129 |
| Zhejiang Lidesen Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 100 |
| Anji Spenq Industrial Co., Ltd. | Huzhou | Zhejiang | Manufacturer | 85 |
Showing 12 of 40. All 40 manufacturers in China registered for Speculum, Vaginal, Nonmetal
Record
| Listed by | Coopersurgical, Inc., United States |
|---|---|
| FDA product code | HIB |
| Device type | Speculum, Vaginal, Nonmetal |
| Device class | Class 2 |
| Regulation | 21 CFR 884.4530 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K920803 |
| Record published | 2016-07-29 |
| Record revised | 2024-02-28 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 12 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 6050T | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Welch Allyn, Inc. | Welch Allyn, Inc. | 30 |
| Vagispec Kolplast | Kolplast C I | 19 |
| EOS | North EOS Industries, Inc. | 19 |
| Shengbo | Yuhuan City Shengbo Mould Manufacturing Co., Ltd. | 18 |
| Centurion | Centurion Medical Products Corporation | 13 |
| ClearSpec | Clearspec, LLC | 12 |
| Speculux | Evexar Medical Limited | 12 |
| McKesson. | Mckesson Medical-Surgical Inc. | 11 |
| Instraspec | Robinson Healthcare Limited | 10 |
| PremierPro | Prestige Ameritech | 9 |
| Bioseal Inc. | Bioseal | 9 |
| ER-Spec/Office-Spec | OBP Medical Corporation | 6 |
Showing 12 of 75. All products under Speculum, Vaginal, Nonmetal
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K951898 | 1995-12-11 |
Recalls Naming This Product
3 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 |
|---|---|---|---|---|---|---|
| Coopersurgical, Inc. | 510(k) number | 2025-06-11 | Class II | Under Investigation by firm | The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile. | 171 units |
| Coopersurgical, Inc. | 510(k) number | 2025-06-11 | Class II | Under Investigation by firm | The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile. | 991 units |
| Coopersurgical, Inc. | 510(k) number | 2025-06-11 | Class II | Under Investigation by firm | The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile. | 475 units |
Recalls
1 of these is 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 |
|---|---|---|---|---|---|
| 2015-04-13 | Class II | Packaging change control | Small sized specula were incorrectly packaged in printed bags for the medium sized speculum | 9400 units | 2016-02-05 |
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.