Data / Medical devices / United States / Greer Medical, Inc.
Greer Medical, Inc.: FDA-registered device maker in Santa Barbara, CA, United States, 1 510(k) clearance
Greer Medical, Inc. is registered with the FDA (registration 2028175) in Santa Barbara, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 28, 1991. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2028175
- FEI number
- 1000125440
- Address
- 201 N. Calle Cesar Chavez Suite 104, Santa Barbara, CA, United States, 93103
- Owner or operator
- Greer Medical, Inc. (10027179)
- Roles
- Specification developer
- First device listed
- October 9, 2008
- Registered through
- 2026
- Brand names listed
- Sapphire Suction Rerservoir, SeromaCath, SurgiFish
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Specification developer | accessdata.fda.gov |
| Retainer, Surgical | GCZ | 1 | 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 |
|---|---|---|---|---|---|---|
| January 28, 1991 | K905733 | SEROMA-CATH CLOSE DRAINAGE SYSTEM | GCY | Substantially Equivalent | Dawn Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Retainer, Surgical
- All makers of Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Updated January 28, 1991. 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.