Data / Medical devices / United States / Greensleeve Medical Corp.
Greensleeve Medical Corp.: FDA-registered device maker in Boerne, TX, United States, 1 510(k) clearance
Greensleeve Medical Corp. is registered with the FDA (registration 3024785124) in Boerne, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 30, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3024785124
- Address
- 624 N Main Street Suite 204, Boerne, TX, United States, 78006
- Owner or operator
- GreenSleeve Medical Corp. (10086356)
- Roles
- Manufacturer
- First device listed
- November 2, 2022
- Registered through
- 2026
- Brand names listed
- GreenSleeve Trocar System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laparoscope, Gynecologic (And Accessories) | HET | 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 |
|---|---|---|---|---|---|---|
| January 30, 1997 | K964436 | WESTERN SURGICAL REUSABLE LAPAROSCOPIC TROCAR SYSTEM | HET | Substantially Equivalent | Western Surgical Instrument Co. | accessdata.fda.gov |
Compare with other makers
Updated January 30, 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.