Resource
MG Ochsner-Dixon Artery Fcps 1 X 2 160MM
99manufacturers in China registered for this device type
32catalogue numbers in this listing
1recall
Who Else Makes It
Concentrated in Zhejiang (34), Jiangsu (25), Shanghai (9). 14 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shanghai Joy Crown Industry Co., Ltd. | Pu Dong New Area | Shanghai | Contract manufacturer | 64 |
| Amsino Medical (Kunshan) Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 53 |
| Flexicare Medical (Dongguan) Ltd. | Dongguan | Guangdong | Contract manufacturer | 48 |
| B.Braun Medical (Suzhou) Co,.Ltd | Suzhou | Jiangsu | Contract manufacturer | 37 |
| Suzhou Microport Orthorecon Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 31 |
| Planet (Anhui) Medical Products Co., Ltd. | Chuzhou | Anhui | Contract manufacturer | 30 |
| Jingmen Huasheng Asia Dynamics Sanitary Products Co., Ltd. | Jingmen | Hubei | Contract manufacturer | 23 |
| Yiwu Haoding Medical Co., Ltd. | Yiwu | Zhejiang | Contract manufacturer | 23 |
| Zhejiang Changdi Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 16 |
| Linhai Deyi Plastic Co., Ltd. | Linhai | Zhejiang | Contract manufacturer | 15 |
| Nantong City Yojo Medical Products Co., Ltd. | Haimen | Jiangsu | Contract manufacturer | 14 |
| Meifu Medical Technology Suzhou Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 13 |
Showing 12 of 99. All 99 manufacturers in China registered for Forceps
Record
| Listed by | Aesculap AG, Germany |
|---|---|
| FDA product code | HTD |
| Device type | Forceps |
| Device class | Class 1 |
| Regulation | 21 CFR 878.4800 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2020-05-08 |
| Record revised | 2022-06-10 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| Distribution end date | 2026-07-08 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| BF463ZR | In distribution | |
| FO610ZR | In distribution | |
| MB231ZR | In distribution | |
| FB404ZR | In distribution | |
| MD450ZR | In distribution | |
| EB004ZR | In distribution | |
| BF120ZR | In distribution | |
| BF113ZR | In distribution | |
| BF122ZR | In distribution | |
| BF458ZR | In distribution | |
| OF411ZR | In distribution | |
| FO620ZR | In distribution | |
| BD225ZR | In distribution | |
| BH131ZR | In distribution | |
| EA037ZR | In distribution | |
| BH618ZR | Withdrawn | |
| BH425ZR | Withdrawn | |
| BD335ZR | Withdrawn | |
| BD027ZR | Withdrawn | |
| BD331ZR | Withdrawn | |
| BD512ZR | Withdrawn | |
| AN909ZR | Withdrawn | |
| BF460ZR | Withdrawn | |
| BD560ZR | Withdrawn | |
| FO640ZR | Withdrawn | |
| EO422ZR | Withdrawn | |
| FO148ZR | Withdrawn | |
| BF432ZR | Withdrawn | |
| MD469ZR | Withdrawn | |
| EA052ZR | Withdrawn | |
| BD537ZR | Withdrawn | |
| BJ072ZR | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Surgical Direct | Surgical Direct, Inc. | 1,186 |
| Aesculap | Aesculap AG | 727 |
| Wexler Surgical, Inc. | Wexler Surgical, Inc. | 636 |
| HNM Medical | HNM Stainless, LLC. | 400 |
| Millennium | Avalign Technologies, Inc. | 365 |
| Forceps | Synthes Gmbh | 296 |
| Princeton | Princeton Medical Group, Inc. | 271 |
| MSI Precision Specialty Instruments | MED Saver, Inc. | 265 |
| Ambler Surgical | Ambler Surgical, LLC | 212 |
| Zoll-Dental | Zoll-Dental | 187 |
| Forceps | George Tiemann & Co. | 184 |
| Anmuth Medical International | Anmuth Medical International LLC | 174 |
Showing 12 of 963. All products under Forceps
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 |
|---|---|---|---|---|
| 2025-01-31 | Class II | Use error | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. | 93,714 forceps |
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.