Data / Medical devices / Japan / Robert Reid Inc.
Robert Reid Inc.: FDA-registered device maker in Tokyo, Japan, 2 510(k) clearances
Robert Reid Inc. is registered with the FDA (registration 3008198024) in Tokyo, Japan. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 15, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008198024
- Address
- 1-1-2 Heiwajima, 6F Ota-ku, Tokyo, Japan, 143-8530
- Owner or operator
- Robert Reid Inc. (10031263)
- Roles
- Specification developer
- First device listed
- January 7, 2010
- Registered through
- 2026
- Brand names listed
- KAPSS Spinal System, Magnum Nail
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Appliance, Fixation, Spinal Interlaminal | KWP | 2 | Specification developer | accessdata.fda.gov |
| Orthosis, Spinal Pedicle Fixation | MNI | 2 | Specification developer | accessdata.fda.gov |
| Orthosis, Spondylolisthesis Spinal Fixation | MNH | 2 | Specification developer | accessdata.fda.gov |
| Rod, Fixation, Intramedullary And Accessories | HSB | 2 | 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 15, 2010 | K093833 | KAPSS SPINAL SYSTEM | MNI | Substantially Equivalent | Robert Reid, Inc. | accessdata.fda.gov |
| November 13, 2009 | K093089 | MAGNUM NAIL | HSB | Substantially Equivalent | Robert Reid, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Rod, Fixation, Intramedullary And Accessories
- All makers of Appliance, Fixation, Spinal Interlaminal
- All makers of Orthosis, Spondylolisthesis Spinal Fixation
- All makers of Orthosis, Spinal Pedicle Fixation
Updated October 15, 2010. 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.