Data / Medical devices / Japan / Top Corporation Ohmasu Plant
Top Corporation Ohmasu Plant: FDA-registered device maker in ISHIOKA Ibaraki, Japan, 1 510(k) clearance
Top Corporation Ohmasu Plant is registered with the FDA (registration 3011500374) in ISHIOKA Ibaraki, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 7, 1984. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011500374
- Address
- 1-5 Ohmasu, ISHIOKA Ibaraki, Japan, 315-0101
- Owner or operator
- TOP CORPORATION (8030272)
- Roles
- Manufacturer
- First device listed
- March 2, 2008
- Registered through
- 2026
- Brand names listed
- NRFit Syringe, TOP HYPODERMIC SYRINGE LUER LOCK
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 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 |
|---|---|---|---|---|---|---|
| December 7, 1984 | K843415 | TOP HYPODERMIC SYRINGE LUER LOCK | FMF | Substantially Equivalent | Top Surgical Manufacturers Co. | accessdata.fda.gov |
Compare with other makers
Updated December 7, 1984. 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.