Company ยท US
Orthomerica Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2024. Name variants (Inc, Corp, punctuation) are merged.
21510(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 |
|---|---|---|---|
| Mar 15, 2024 | K240466 | STARband 3D Orthomerica Products, Inc. | OAN |
| Apr 20, 2023 | K223238 | STARband 3D Orthomerica Products, Inc. | MVA |
| Aug 17, 2021 | K211376 | STARband Orthomerica Products, Inc. | OAN |
| Apr 27, 2021 | K203098 | STARband, STARlight, St. Louis Band Orthomerica Products, Inc. | OAN |
| Mar 1, 2018 | K180109 | STARband, STARlight, St. Louis Band Orthomerica Products, Inc. | OAN |
| Jul 20, 2016 | K161138 | St. Louis Band Orthomerica Products, Inc. | OAN |
| Sep 18, 2015 | K151979 | STARband, STARlight Orthomerica Products, Inc. | OAN |
| Jul 1, 2015 | K151147 | STARband, STARlight Orthomerica Products, Inc. | OAN |
| Apr 23, 2015 | K142141 | STARBAND, STARLIGHT Orthomerica Products, Inc. | OAN |
| Oct 6, 2014 | K141842 | STARBAND, STARLIGHT Orthomerica Products, Inc. | MVA |
| Jun 6, 2014 | K140353 | STARBAND AND STARLIGHT Orthomerica Products, Inc. | MVA |
| Jan 16, 2014 | K133250 | STARLIGHT Orthomerica Products, Inc. | OAN |
| Jun 10, 2013 | K124023 | STARBAND Orthomerica Products, Inc. | OAN |
| Jul 17, 2009 | K090587 | STARLIGHT Orthomerica Products, Inc. | OAN |
| Dec 5, 2008 | K082950 | STARBAND Orthomerica Products, Inc. | OAN |
| Oct 31, 2008 | K082945 | STARLIGHT Orthomerica Products, Inc. | OAN |
| Sep 12, 2008 | K081994 | STARLIGHT Orthomerica Products, Inc. | OAN |
| Jul 25, 2002 | K021918 | CLARREN HELMET (ORTHOMERICA) Orthomerica Products, Inc. | OAN |
| Jul 9, 2002 | K021207 | STARLIGHT Orthomerica Products, Inc. | OAN |
| Jul 3, 2001 | K011350 | STARBAND CRANIAL ORTHOSIS Orthomerica Products, Inc. | OAN |
| Jul 7, 2000 | K001167 | OPI BAND Orthomerica Products, Inc. | MVA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||