Data / Medical devices / Japan / Keisei Medical Industrial Co., Ltd.
Keisei Medical Industrial Co., Ltd.: FDA-registered device maker in BUNKYO-KU Tokyo, Japan, 2 510(k) clearances
Keisei Medical Industrial Co., Ltd. is registered with the FDA (registration 9611484) in BUNKYO-KU Tokyo, Japan. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 30, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9611484
- FEI number
- 3002807390
- Address
- 19-6, Hongo Sanchome, BUNKYO-KU Tokyo, Japan, 113-0033
- Owner or operator
- KEISEI MEDICAL INDUSTRIAL CO., LTD. (8031595)
- Roles
- Manufacturer
- First device listed
- December 30, 1986
- Registered through
- 2026
- Brand names listed
- Keisei Medical
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Air Fluidized | INX | 2 | Manufacturer | accessdata.fda.gov |
| Clamp, Vascular | DXC | 2 | Manufacturer | accessdata.fda.gov |
| Dermatome | GFD | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Manufacturer | accessdata.fda.gov |
| Microscope, Surgical | EPT | 1 | Manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polyamide | GAR | 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 |
|---|---|---|---|---|---|---|
| March 30, 2000 | K993970 | MICRINS MICROSURGICAL SUTURE | GAR | Substantially Equivalent | Micrins Surgical, Inc. | accessdata.fda.gov |
| March 26, 1999 | K982278 | MICRINS MICRO ANASTOMOSIS CLAMP | DXC | Substantially Equivalent | Micrins Surgical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Suture, Nonabsorbable, Synthetic, Polyamide
- All makers of Bed, Air Fluidized
- All makers of Clamp, Vascular
- All makers of Dermatome
- All makers of Instrument, Surgical, Disposable
- All makers of Microscope, Surgical
Updated March 30, 2000. 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.