Data / Medical devices / China / B.j.zh.f.panther Medical Equipment Co.,ltd
B.j.zh.f.panther Medical Equipment Co.,ltd: FDA-registered device maker in Beijing, China, 3 510(k) clearances
B.j.zh.f.panther Medical Equipment Co.,ltd is registered with the FDA (registration 3008388437) in Beijing, China. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 12, 2015. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3008388437
- Address
- No. 8 Shangcheng Road, Beiqijia Changping District, Beijing, China, 102209
- Owner or operator
- B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO.,LTD (10032615)
- Roles
- Manufacturer
- First device listed
- June 1, 2010
- Registered through
- 2027
- Brand names listed
- PANTHER Cutter Stapler, Panther, Panther Endo Linear Cutter Staplers With Single Use Loading Units, Panther Skin Stapler, Panther Skin Stapler Remover
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suturing, Stomach And Intestinal | FHM | 1 | Manufacturer | accessdata.fda.gov |
| Staple, Implantable | GDW | 2 | Manufacturer | accessdata.fda.gov |
| Staple, Removable (Skin) | GDT | 1 | Manufacturer | accessdata.fda.gov |
| Stapler, Skin | QQS | 1 | Manufacturer | accessdata.fda.gov |
| Stapler, Surgical | GAG | 2 | 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 |
|---|---|---|---|---|---|---|
| November 12, 2015 | K152618 | PANTHER Cutter Stapler | GDW | Substantially Equivalent | B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO., Ltd. | accessdata.fda.gov |
| June 11, 2015 | K142577 | PANTHER Endo Linear Cutter Staplers with Single Use Loading Units | GDW | Substantially Equivalent | B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO., Ltd. | accessdata.fda.gov |
| January 11, 2011 | K103470 | PANTHER GROUP OF SURGICAL INCLUDES: OANTHER CIRCULAR STAPLER; PANTHER HEMORRHOIDAL CIRCULAR STAPLER; PANTHER LINEAR STAP | GDW | Substantially Equivalent | B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Staple, Removable (Skin)
- All makers of Apparatus, Suturing, Stomach And Intestinal
- All makers of Staple, Implantable
- All makers of Stapler, Surgical
- All makers of Stapler, Skin
Updated November 12, 2015. 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.