Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled 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 Medicel AG with 6 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Sep 16, 2025: ACCUJECT Injector Set 2.1-1P (LP604590).
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 16, 2025 | ACCUJECT Injector Set 2.1-1P (LP604590)K252540 · MSS | 510(k) clearances |
| Sep 19, 2023 | Accuject Refra Injector AR2900K231106 · MSS | 510(k) clearances |
| Aug 5, 2013 | Product Name: nanoPOINT Injector System, item number 37-0000-08. Intended to fold and insert a STAAR Surgical Collamer¿ nanoFLEX or AfiniClass II · The firm initiated this recall of one lot (121402) of nanoPOINT Injectors after they noticed that Tyvek lids might have | Device recalls |
| Aug 9, 2010 | VISIAN NANOPOINT 2.0 INJECTOR MODEL LP604430K101134 · MSS | 510(k) clearances |
| Jul 28, 2009 | NAVIJECT SUB2-1P, MODEL: LP604430K092023 · MSS | 510(k) clearances |
| Nov 1, 2007 | IOL INJECTOR SETK070669 · KYB | 510(k) clearances |
| Jun 17, 2004 | MULTIJECT INJECTOR AND MICROGLIDE CARTRIDGEK040837 · MSS | 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
