Company ยท US
Meditrina, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2019 to 2023. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| HIH | Hysteroscope (And Accessories) | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 21, 2023 | K223813 | Aveta System 2.0 Meditrina, Inc. | HIH |
| May 26, 2022 | K213171 | Aveta System, Aveta Disposable Hysteroscope (Pearl/Opal/Coral), Aveta Disposable Cystoscope (Coral) Meditrina, Inc. | HIH |
| Dec 19, 2019 | K192100 | Aveta Disposable Hysteroscope Meditrina, Inc. | HIH |
| Oct 1, 2019 | K191958 | Aveta System Meditrina, Inc. | HIH |
| May 16, 2019 | K190372 | Aveta System Meditrina, Inc. | HIH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||