Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list seca with 5 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jan 23, 2020: Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535.
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.
| Jan 23, 2020 | Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535K192092 · DXN | 510(k) clearances |
| Jun 19, 2019 | Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009Class II · It has been determined that the wheels on the baby scale cart can unexpectedly loosen and in the worst case, detach from | Device recalls |
| May 2, 2013 | SECA MEDICAL BODY COMPOSTION ANALYZER 514, SECA MBCA 514, SECA MBCA, SECA 514K122388 · MNW | 510(k) clearances |
| Jul 30, 1982 | SECA DIGITAL BABY SCALE 727K822135 · FRW | 510(k) clearances |
| Jul 28, 1982 | SECA LIGHT WEIGHT BABY SCALE 744K822042 · FRW | 510(k) clearances |
| Jul 28, 1982 | SECA CHAIR SCALE-721K822043 · FRW | 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
