Data / Medical devices / Canada / Adaptiiv Medical Technologies, Inc.
Adaptiiv Medical Technologies, Inc.: FDA-registered device maker in Halifax Nova Scotia, Canada, 5 510(k) clearances
Adaptiiv Medical Technologies, Inc. is registered with the FDA (registration 3014873236) in Halifax Nova Scotia, Canada. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated February 19, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014873236
- Address
- 1559 Barrington Street Suite 200-D, Halifax Nova Scotia, Canada, B3J 1Z8
- Owner or operator
- Adaptiiv Medical Technologies, Inc. (10058427)
- Roles
- Manufacturer
- First device listed
- September 27, 2018
- Registered through
- 2026
- Brand names listed
- Nova Surface Applicator, Patient-Matched 3D Printed Radiation Therapy Accessory, TrueFit Bolus, TrueFlex Bolus
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Planning, Radiation Therapy Treatment | MUJ | 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 |
|---|---|---|---|---|---|---|
| February 19, 2026 | K260308 | TrueFit Bolus | MUJ | Substantially Equivalent | Adaptiiv Medical Technologies, Inc. | accessdata.fda.gov |
| October 23, 2024 | K243057 | TrueFit Bolus; TrueFlex Bolus | MUJ | Substantially Equivalent | Adaptiiv Medical Technologies, Inc. | accessdata.fda.gov |
| August 30, 2024 | K241318 | Nova Surface Applicator (ADPT-ONDEM-3DPRT-BRA) | MUJ | Substantially Equivalent | Adaptiiv Medical Technologies, Inc. | accessdata.fda.gov |
| January 19, 2022 | K213438 | 3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory | MUJ | Substantially Equivalent | Adaptiiv | accessdata.fda.gov |
| July 10, 2018 | K180289 | 3D Bolus Software | MUJ | Substantially Equivalent | 3D Bolus, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 19, 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.