Data / Medical devices / United States / Cimetra LLC
Cimetra LLC: FDA-registered device maker in West Chazy, NY, United States, 6 510(k) clearances
Cimetra LLC is registered with the FDA (registration 1317927) in West Chazy, NY, United States. It lists 2 device types. The FDA files 6 510(k) clearances under its listings, the newest dated October 2, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1317927
- Address
- 8396 State Route 9, West Chazy, NY, United States, 12992
- Owner or operator
- CIMETRA LLC. (1317927)
- Roles
- Repackager or relabeler
- First device listed
- November 10, 1983
- Registered through
- 2026
- Brand names listed
- 100 Triodes AG/AGCL, AV Sync Sensor, Bend Sensor Adapter, Biofun Games, Biograph Infi SW upgrade, Biograph Infi SW upgrade Spanish, Biograph Infiniti Developers tools SW, Biograph Infiniti NATS Software and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Biofeedback | HCC | 2 | Repackager or relabeler | accessdata.fda.gov |
| Perineometer | HIR | 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 |
|---|---|---|---|---|---|---|
| October 2, 1997 | K972723 | BIO TROL | HCC | Substantially Equivalent | Mindmedia Labs, Inc. | accessdata.fda.gov |
| September 29, 1995 | K925681 | MYOTRAC2D/CS | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| May 11, 1995 | K935213 | INCONTROL | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| May 11, 1995 | K932149 | THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| February 12, 1991 | K903497 | FLEXCOMP DSP & PROCOMP | HCC | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| September 26, 1988 | K881416 | MYOTRAC | HCC | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 2, 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.