Data / Medical devices / System, Imaging, Pulsed Echo, Ultrasonic / Singapore
FDA-registered makers of System, Imaging, Pulsed Echo, Ultrasonic in Singapore: 5 establishments
5 establishments in Singapore are registered with the FDA to make System, Imaging, Pulsed Echo, Ultrasonic (product code IYO). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, Imaging, Pulsed Echo, Ultrasonic
- Product code
- IYO
- Country
- Singapore
Makers of System, Imaging, Pulsed Echo, Ultrasonic in Singapore
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Biobot Surgical Pte. Ltd. | Singapore South West, Singapore | Manufacturer | 4 | December 21, 2023 | 0 | 0 | 0 | api.fda.gov |
| Flextronics Manufacturing (Singapore) Pte Ltd | SINGAPORE South East, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Circuit (Singapore) Pte Ltd | Singapore Central Singapore, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smicna Pte Ltd | Singapore Central Singapore, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sys-Mac Automation Engineering Pte Ltd | Singapore North West, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.