Company ยท US
Maxtec, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2023. Name variants (Inc, Corp, punctuation) are merged.
10510(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 |
|---|---|---|---|
| Dec 4, 2023 | K231895 | Maxtec MaxBlend2+p Maxtec, LLC | BZR |
| Apr 1, 2023 | K221734 | Maxtec MaxO2 ME+p Maxtec, LLC | CCL |
| May 23, 2019 | K182362 | MaxCap Ped and MaxCap Neo Maxtec, LLC | CCK |
| Oct 27, 2016 | K161718 | MaxBlend 2, MaxBlend Lite Maxtec, LLC | BZR |
| Jun 10, 2016 | K153659 | MaxO2ME Maxtec, LLC | CCL |
| Mar 28, 2014 | K133540 | FLOCAP Maxtec, Inc. | CCK |
| Mar 1, 2012 | K113232 | MAXMIXING BLOCK Maxtec, Inc. | BZR |
| Dec 14, 2011 | K112402 | ULTRAMAXO2 OXYGEN ANALYER Maxtec, LLC | CCL |
| Feb 22, 2007 | K063488 | MAXO2 CU Maxtec, Inc. | CCL |
| Jun 9, 2004 | K040484 | MAXO2+, MODEL A AND AE Maxtec, Inc. | CCL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||