Data / Medical devices / Canada / Octostop, Inc.
Octostop, Inc.: FDA-registered device maker in LAVAL Quebec, Canada, 9 510(k) clearances
Octostop, Inc. is registered with the FDA (registration 8022065) in LAVAL Quebec, Canada. It lists 4 device types. The FDA files 9 510(k) clearances under its listings, the newest dated August 14, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8022065
- FEI number
- 3003434037
- Address
- 1675 Boul St-Elzear Ouest, LAVAL Quebec, Canada, H7L 3N6
- Owner or operator
- OCTOSTOP, INC. (8022065)
- Roles
- Manufacturer
- First device listed
- July 24, 1995
- Registered through
- 2026
- Brand names listed
- Shockeez, boomerang, gentle slope, ingot, octopaque, pharaoh, ridges, ridges plus and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cradle, Patient, Radiologic | KXH | 1 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Stationary | KPR | 2 | Manufacturer | accessdata.fda.gov |
| Table, Radiographic, Stationary Top | IXQ | 2 | Manufacturer | accessdata.fda.gov |
| Table, Radiographic, Tilting | IXR | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| August 14, 1997 | K972766 | PIVOTING COMPENSATING FILTERS FOR THE HEAD | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| November 27, 1996 | K963941 | THE PHARAOH COMPENSATING FILTER | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| July 20, 1995 | K952871 | RIDGES PLUS | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| September 6, 1994 | K940306 | OCTOSTOP COMPENSATING FILTERS | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| January 21, 1993 | K926069 | WRIST TRACTION | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| October 14, 1992 | K913711 | GENTLE SLOPE | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| October 14, 1992 | K913659 | LITTLE PRISM | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| September 16, 1991 | K910757 | THE BULLION | KPR | Substantially Equivalent | Octostop, Inc. | accessdata.fda.gov |
| November 15, 1985 | K853330 | BOOMERANG ABSORPTION COMENSATION FILTER | KPR | Substantially Equivalent | Entreprises Octostop, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, X-Ray, Stationary
- All makers of Cradle, Patient, Radiologic
- All makers of Table, Radiographic, Stationary Top
- All makers of Table, Radiographic, Tilting
Updated August 14, 1997. 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.