Company ยท US
Sunmed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2024. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 2, 2024 | K233098 | MYOTouch Muscle Stimulator Sunmed, LLC | IPF |
| Mar 28, 2013 | K121743 | EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN Sunmed, LLC, CN | BXN |
| Nov 14, 2008 | K081805 | CUFFALERT Sunmed | BSK |
| Jun 4, 2007 | K062112 | SUNMED FOLEY CATHETERS Sunmed, Inc. | EZL |
| Feb 27, 1996 | K955632 | ORTHOPLUG SOFT BONE DESIGN Sunmed, Inc. | LZN |
| Feb 27, 1996 | K955631 | ORTHOPLUG HARD BONE DESIGN Sunmed, Inc. | LZN |
| Jun 1, 1993 | K921263 | SUNLITE LARYNGOSCOPE Sunmed, Inc. | CCW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||