Data / Medical devices / Fixation Accessory
Fixation Accessory (LYT): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Fixation Accessory (product code LYT, Class 2, 21 CFR 888.3030). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on April 12, 2004, and lists 2 recall events (0 Class I). FDA data exported November 3, 2026.
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- Product code
- LYT
- Device class
- 2
- Regulation
- 888.3030
- Medical specialty
- Orthopedic
- Implant
- Yes
Makers by country
| Country | Makers |
|---|---|
| Ireland | 3 |
| United States | 2 |
| France | 1 |
Makers of Fixation Accessory
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Jurgan Development & MFG., Ltd. | Madison, WI, United States | Manufacturer | 1 | June 8, 1983 | 0 | 0 | 0 | api.fda.gov |
| Howmedica International S. De R.L. | LIMERICK Munster, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Howmedica Osteonics Corp | Mahwah, NJ, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precera Medical Herouville SAS | HEROUVILLE ST CLAIR CEDEX Normandie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Ireland Osteonics | County Cork, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Anngrove | Cork Munster, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated April 12, 2004. 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.