Data / Medical devices / United States / Cypris Medical, Inc.
Cypris Medical, Inc.: FDA-registered device maker in Evanston, IL, United States, 2 510(k) clearances
Cypris Medical, Inc. is registered with the FDA (registration 3013354263) in Evanston, IL, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 3, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013354263
- Address
- 909 Davis St Ste 500, Evanston, IL, United States, 60201
- Owner or operator
- Cypris Medical, Inc. (10053047)
- Roles
- Specification developer
- First device listed
- April 14, 2017
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Carrier, Ligature | GEJ | 1 | Specification developer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polypropylene | GAW | 2 | Specification developer | accessdata.fda.gov |
| Suture, Surgical, Absorbable, Polydioxanone | NEW | 2 | Specification developer | accessdata.fda.gov |
| Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene | NBY | 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 |
|---|---|---|---|---|---|---|
| May 3, 2024 | K240185 | Cypris eXact Suture Placement Device | GEJ | Substantially Equivalent | Cypris Medical | accessdata.fda.gov |
| January 12, 2024 | K233355 | Cypris eXact Suturing System | GAW | Substantially Equivalent | Cypris Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene
- All makers of Suture, Nonabsorbable, Synthetic, Polypropylene
- All makers of Carrier, Ligature
- All makers of Suture, Surgical, Absorbable, Polydioxanone
Updated May 3, 2024. 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.