Data / Medical devices / Japan / NIPRO VASCULAR CORPORATION Aichi Facility
NIPRO VASCULAR CORPORATION Aichi Facility: FDA-registered device maker in Seto Aichi, Japan, 2 510(k) clearances
NIPRO VASCULAR CORPORATION Aichi Facility is registered with the FDA (registration 3030042169) in Seto Aichi, Japan. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 22, 2025. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3030042169
- Address
- 1-176 Shiokusagaoka, Seto Aichi, Japan, 489-0899
- Owner or operator
- NIPRO VASCULAR CORPORATION (10061300)
- Roles
- Manufacturer
- First device listed
- April 1, 2024
- Registered through
- 2027
- Brand names listed
- Aperta NSE PTA Balloon Dilatation Catheter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Angioplasty, Peripheral, Transluminal | LIT | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous, Cutting/Scoring | PNO | 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 |
|---|---|---|---|---|---|---|
| April 22, 2025 | K243944 | Aperta NSE PTA Balloon Dilatation Catheter | PNO | Substantially Equivalent | Goodman Co., Ltd. | accessdata.fda.gov |
| March 28, 2024 | K232013 | Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040) | PNO | Substantially Equivalent | Goodman Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Percutaneous, Cutting/Scoring
- All makers of Catheter, Angioplasty, Peripheral, Transluminal
Updated April 22, 2025. 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.