Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SingaporeLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medipurpose with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 22, 2022: SurgiLance® Safety Lancet.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 22, 2022 | SurgiLance® Safety LancetK222224 · FMK | 510(k) clearances |
| Feb 11, 2013 | BABYLANCE HEEL INCISION DEVICEK130132 · FMK | 510(k) clearances |
| Sep 1, 2011 | MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AGK110062 · FRO | 510(k) clearances |
| Oct 21, 2010 | SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250K101145 · FMK | 510(k) clearances |
| Oct 19, 2010 | BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200K101417 · FMK | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
