Data / Medical devices / Singapore / NSP Tech Pte Ltd
NSP Tech Pte Ltd: FDA-registered device maker in Singapore Central Singapore, Singapore, 5 510(k) clearances
NSP Tech Pte Ltd is registered with the FDA (registration 3008337059) in Singapore Central Singapore, Singapore. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 24, 2022. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3008337059
- Address
- 10 Admiralty Street Northlink Building, #02-06, Singapore Central Singapore, Singapore, 757695
- Owner or operator
- NSP Tech Pte Ltd (10035435)
- Roles
- Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer, Specification developer
- First device listed
- February 27, 2011
- Registered through
- 2026
- Brand names listed
- Bevel Up Holder (BUH), Blood Collection Accessory (BUCA), Blood Transfer Accessory (BTA), MediHeel, Novaplus, SAFETICET PLUS, SafetiCET Safety Lancet, SafetiHeel
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Specimen Collection Convenience Kit (Excludes Hiv) | PQD | 2 | Manufacturer | accessdata.fda.gov |
| Kit, Screening, Urine | JXA | 1 | Manufacturer | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Complaint file establishment, Exporter to the US, Manufacturer, Specification developer | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer, Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 24, 2022 | K221783 | SafetiCET Safety Lancet | FMK | Substantially Equivalent | Nsp Tech Pte, Ltd. | accessdata.fda.gov |
| August 22, 2022 | K221604 | SafetiHeel, MediHeel, Novaplus | FMK | Substantially Equivalent | Nsp Tech Pte, Ltd. | accessdata.fda.gov |
| April 21, 2020 | K193074 | Bevel Up Holder | JKA | Substantially Equivalent | Nsp Tech Pte, Ltd. | accessdata.fda.gov |
| July 30, 2019 | K181754 | Blood Collection Accessory (BUCA) | JKA | Substantially Equivalent | Nsp Tech Pte, Ltd. | accessdata.fda.gov |
| July 30, 2019 | K181743 | Blood Transfer Accessory (BTA) | JKA | Substantially Equivalent | Nsp Tech Pte, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- All makers of Kit, Screening, Urine
- All makers of Blood Specimen Collection Convenience Kit (Excludes Hiv)
Updated October 24, 2022. 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.