Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Creo Medical with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 6, 2025: SpydrBlade Flex Instrument (PRD-RG1-001).
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.
| Jun 6, 2025 | SpydrBlade Flex Instrument (PRD-RG1-001)K242774 · KNS | 510(k) clearances |
| Feb 5, 2025 | CROMA Electrosurgical Generator (PRD-EMR-050)K242983 · GEI | 510(k) clearances |
| Aug 15, 2024 | Reusable Interface Cable 1.5 m (PRD-IFC-002)K242061 · KNS | 510(k) clearances |
| Oct 31, 2023 | Speedboat Flush SB1 InstrumentK230328 · KNS | 510(k) clearances |
| Jun 26, 2023 | AB1 Electrosurgical Instrument, Creo Electrosurgical SystemK223138 · NEY | 510(k) clearances |
| Feb 14, 2023 | Creo Electrosurgical System with NP1 InstrumentK221672 · NEY | 510(k) clearances |
| Jan 5, 2021 | ABI Instrument, Creo Electrosurgical SystemK200298 · NEY | 510(k) clearances |
| Oct 28, 2020 | NP1 Instrument, Creo Electrosurgical SystemK200003 · NEY | 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
