Data / Medical devices / Orthosis, Corrective Shoe / Indonesia
FDA-registered makers of Orthosis, Corrective Shoe in Indonesia: 5 establishments
5 establishments in Indonesia are registered with the FDA to make Orthosis, Corrective Shoe (product code KNP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Orthosis, Corrective Shoe
- Product code
- KNP
- Country
- Indonesia
Makers of Orthosis, Corrective Shoe in Indonesia
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Multi Garmen Indonesia | BOGOR Jawa Barat, Indonesia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PT. Cipta Karya Buana | Sidoarjo Jawa Timur, Indonesia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PT. Parkland World Indonesia 2 | Serang Banten, Indonesia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PT. Seng Dam Jaya Abadi | Mojokerto Jawa Timur, Indonesia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PT. Sukses Abadi Indonesia | Kabupaten Nganjuk Jawa Timur, Indonesia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.