Data / Medical devices / China / Hubei Qianjiang Kingphar Medical Material Co., Ltd
Hubei Qianjiang Kingphar Medical Material Co., Ltd: FDA-registered device maker in Qianjiang, Hubei, China, 1 510(k) clearance
Hubei Qianjiang Kingphar Medical Material Co., Ltd is registered with the FDA (registration 9616872) in Qianjiang, Hubei, China. It lists 52 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 19, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9616872
- FEI number
- 3002897187
- Address
- Yuanguang Road., Qianjiang, Hubei, China, 433100
- Owner or operator
- HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD (9041777)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- June 8, 2000
- Registered through
- 2026
- Brand names listed
- ABSORBENT TIPPED APPLICATOR, APRON, PROTECTIVE, Air Water Syringe Tips, BANDAGE COMPRESSION, Baby bibs, Barrier covers, Barrier film, Cast Bandage; Orthopedic Bandage; Plaster Bandage; POP Bandage; undercast padding and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Absorber, Saliva, Paper | KHR | 1 | Manufacturer | accessdata.fda.gov |
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Non-Sterile | KXF | 1 | Manufacturer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Sterile | KXG | 1 | Manufacturer | accessdata.fda.gov |
| Apron, Protective | IWO | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Bag, Ice | KYR | 1 | Manufacturer | accessdata.fda.gov |
| Bandage, Cast | ITG | 1 | Manufacturer | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Bandage, Liquid, Skin Protectant | NEC | 1 | Manufacturer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Cap, Surgical | FYF | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Cotton, Roll | EFN | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Limb | IPM | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Mattress (Medical Purposes) | FMW | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Cover, Shoe, Operating-Room | FXP | 1 | Manufacturer | accessdata.fda.gov |
| Dental Hygiene Kit | NXZ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Manufacturer | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Manufacturer | accessdata.fda.gov |
| Dressing, Compression | MHW | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Evacuator, Oral Cavity | EHZ | 1 | Manufacturer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Manufacturer | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Manufacturer | accessdata.fda.gov |
| Gauze/Sponge, Internal, X-Ray Detectable | GDY | 1 | Manufacturer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Manufacturer | accessdata.fda.gov |
| Holder, Ureteral Catheter | EYJ | 1 | Manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Kit, Surgical Instrument, Disposable | KDD | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Mouthpiece, Saliva Ejector | DYN | 1 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Manufacturer | accessdata.fda.gov |
| Pad, Alcohol, Device Disinfectant | LKB | U | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pad, Eye | HMP | 1 | Manufacturer | accessdata.fda.gov |
| Patient Personal Hygiene Kit | NSB | 1 | Manufacturer | accessdata.fda.gov |
| Personal Protection Kit | PXC | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Sling, Arm | ILI | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Stocking, Elastic | ILG | 1 | Manufacturer | accessdata.fda.gov |
| Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) | DWL | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Periodontic, Endodontic, Irrigating | EIC | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Syringe, Air And/Or Water | ECB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wound Dressing Kit | MCY | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 2 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| July 19, 2022 | K220777 | Surgical face mask | FXX | Substantially Equivalent | Hubei Qianjiang Kingphar Medical Material Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 19, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.