Data / Medical devices / Thailand / Nitta M&T (thailand) Co Ltd
Nitta M&T (thailand) Co Ltd: FDA-registered device maker in A.Sung Noen Nakhon Ratchasima, Thailand, 1 510(k) clearance
Nitta M&T (thailand) Co Ltd is registered with the FDA (registration 3021014160) in A.Sung Noen Nakhon Ratchasima, Thailand. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 14, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021014160
- Address
- Nava Nakorn II Industrial Estate 999/16 Moo 1, T.Na Klang, A.Sung Noen Nakhon Ratchasima, Thailand, 30170
- Owner or operator
- Nitta M&T (Thailand) Co Ltd (10083226)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer
- First device listed
- November 3, 2021
- Registered through
- 2026
- Brand names listed
- 0.2L Safety Box NT-008, 1.5Qts. Safety Box NT-023, 1L Safety Box NT-001, 3.2L Safety Box Rotate Lid NT-006, 5L Safety Box NT-004, 7.6L Safety Box NT-005, 7.6L Safety Box NT-007, 77248 1L SS pole Bracket and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Complaint file establishment, Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| September 14, 2021 | K211464 | Nitta M&T Safety Box | MMK | Substantially Equivalent | Nitta M&T (Thailand) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 14, 2021. 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.