Data / Medical devices / United States / Thompson Mis
Thompson Mis: FDA-registered device maker in Sandown, NH, United States, 1 510(k) clearance
Thompson Mis is registered with the FDA (registration 3009404219) in Sandown, NH, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 26, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009404219
- Address
- 17 Bobcat Way Unit 7, Sandown, NH, United States, 03873
- Owner or operator
- Thompson MIS (10038982)
- Roles
- Specification developer
- First device listed
- November 30, 2011
- Registered through
- 2026
- Brand names listed
- BoneBac Press, BoneBac TLIF Mallet, BoneBac TLIF Surgical Instrument, Nautilus One Step Dilator, Thompson MIS BoneBac TPLIF
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Curette | HTF | 1 | Specification developer | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Lumbar | MAX | 2 | Specification developer | accessdata.fda.gov |
| Mallet | HXL | 1 | Specification developer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Specification developer | accessdata.fda.gov |
| Retractor | GAD | 1 | Specification developer | accessdata.fda.gov |
| Trap, Sterile Specimen | BYZ | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 26, 2011 | K111512 | BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM | MAX | Substantially Equivalent | Thompson Mis, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Curette
- All makers of Retractor
- All makers of Intervertebral Fusion Device With Bone Graft, Lumbar
- All makers of Orthopedic Manual Surgical Instrument
- All makers of Trap, Sterile Specimen
- All makers of Mallet
Updated October 26, 2011. 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.