Medical device makerLabelled 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 14, 2026, FDA's public records list SRA Developments, Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 2022: LOTUS Series 4 Enhanced Shears, LOTUS Series 5.
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.
| Dec 15, 2022 | LOTUS Series 4 Enhanced Shears, LOTUS Series 5K221102 · LFL | 510(k) clearances |
| Jul 17, 2015 | Lotus Series 4 Ultrasonic Surgical System & AccessoriesK151101 · LFL | 510(k) clearances |
| Dec 19, 2007 | LOTUS ULTRASONIC SYSTEM FOR CEMENTED IMPLANT EXTRACTION (USCIX)K072961 · JDX | 510(k) clearances |
| Feb 22, 2007 | SERIES 3 LOTUS LAPAROSCOPIC ULTRASOUND SURGERY SYSTEMK063531 · LFL | 510(k) clearances |
| Dec 16, 2003 | LOTUSK032424 · LFL | 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
