Data / Medical devices / Orthopedic Manual Surgical Instrument / Canada
FDA-registered makers of Orthopedic Manual Surgical Instrument in Canada: 6 establishments
6 establishments in Canada are registered with the FDA to make Orthopedic Manual Surgical Instrument (product code LXH). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Orthopedic Manual Surgical Instrument
- Product code
- LXH
- Country
- Canada
Makers of Orthopedic Manual Surgical Instrument in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| A7 Integration | Granby Quebec, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Batrik Medical Manufacturing Inc. | Lachine Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bodycad Laboratories, Inc. | Quebec, Canada | Complaint file establishment, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Orthopediatrics Canada ULC | Laval Quebec, Canada | Manufacturer | 0 | 0 | 3 | 0 | api.fda.gov | |
| SPINOLOGICS, INC. also DBA Spino Modulation Inc and Numalogics Inc | Montreal Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer Cas | Montreal, Quebec, Canada | Manufacturer, Specification developer | 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.