Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list FMD Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 20, 2026: FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Pe….
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.
| Mar 20, 2026 | FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40K260544 · DQX | 510(k) clearances |
| Jun 13, 2024 | FMD Peripheral Guide Wire F-18 Flex 400 (CSU415400259)K240460 · DQX | 510(k) clearances |
| May 27, 2022 | FMD Peripheral Guide Wires F-14 and F-18, FMD Guide Wire Extension F-14 EXTK212268 · DQX | 510(k) clearances |
| Oct 12, 2004 | TWINHEADS TH-103 EXTRACORPOREAL SHOCK WAVE LITHOTRIPTERK042561 · LNS | 510(k) clearances |
| May 2, 2003 | TWINHEADS TH-101 EXTRACORPOREAL SHOCK WAVE LITHOTRIPTERK030346 · LNS | 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
