Data / Medical devices / United Kingdom / Hunt Developments (uk) Limited
Hunt Developments (uk) Limited: FDA-registered device maker in Midhurst West Sussex, United Kingdom, 4 510(k) clearances
Hunt Developments (uk) Limited is registered with the FDA (registration 3005652161) in Midhurst West Sussex, United Kingdom. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 30, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005652161
- Address
- Unit 17 Holmbush Industrial Estate, Midhurst West Sussex, United Kingdom, GU29 9HX
- Owner or operator
- Hunt Developments (UK) Limited (10045954)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- January 16, 2014
- Registered through
- 2026
- Brand names listed
- Nasosorption FX.i, Tuke saw
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Absorbent Tipped, Non-Sterile | KXF | 1 | Manufacturer | accessdata.fda.gov |
| Blade, Saw, General & Plastic Surgery, Surgical | GFA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Filler, Bone Void, Calcium Compound | MQV | 2 | Repackager or relabeler | accessdata.fda.gov |
| Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | JWH | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| June 30, 2020 | K201464 | Altapore MIS | MQV | Substantially Equivalent | Baxter Healthcare Corporation | accessdata.fda.gov |
| January 9, 2020 | K192363 | Altapore | MQV | Substantially Equivalent | Baxter Healthcare Corporation | accessdata.fda.gov |
| August 17, 2018 | K181306 | Actifuse Flow | MQV | Substantially Equivalent | Baxter Healthcare Corporation | accessdata.fda.gov |
| November 25, 2008 | K082575 | ACTIFUSE BONE GRAFT SUBSTITUTE AND ABX E-Z-FIL AND SHAPE BONE GRAFT SUBSTITUTES | MQV | Substantially Equivalent | Apatech , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Filler, Bone Void, Calcium Compound
- All makers of Applicator, Absorbent Tipped, Non-Sterile
- All makers of Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- All makers of Blade, Saw, General & Plastic Surgery, Surgical
Updated June 30, 2020. 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.