Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Thermo Fisher ScientificLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Life Technologies with 23 device recalls and 11 510(k) clearances. The most recent is a 510(k) clearance dated Oct 15, 2026: Oncomine ™ Dx Express Test.
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.
| Oct 15, 2026 | Oncomine ™ Dx Express TestK260827 · SBY | 510(k) clearances |
| Jan 8, 2025 | Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select PanelK241806 · QOF | 510(k) clearances |
| Jul 10, 2024 | Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR KitK233453 · QQX | 510(k) clearances |
| Feb 21, 2020 | Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic AnalyzerK191030 · PCA | 510(k) clearances |
| Aug 24, 2018 | Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050), for In-Vitro Diagnostic UseClass II · Leaky bottles due to a defect in the bottle cap compromising the sterility of the product | Device recalls |
| Aug 24, 2018 | Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061Class II · Leaky bottles due to a defect in the bottle cap compromising the sterility of the product | Device recalls |
| Aug 24, 2018 | Gibco DPBS, calcium, magnesium, for In-Vitro Diagnostic Use SKU 14040141Class II · Leaky bottles due to a defect in the bottle cap compromising the sterility of the product | Device recalls |
| Aug 24, 2018 | Gibco Sodium Pyruvate (100 mM) SKU 11360070, for In-Vitro Diagnostic UseClass II · Leaky bottles due to a defect in the bottle cap compromising the sterility of the product | Device recalls |
| May 10, 2018 | GIBCO CTS AIM V Serum-Free Media (SFM), Model Number 0870112BK. Tissue and cell culture medium.Class II · It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. | Device recalls |
| May 10, 2018 | Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, Model Number 11965175. Tissue and cell culture medium.Class II · It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. | Device recalls |
| May 10, 2018 | Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell culture medium.Class II · It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. | Device recalls |
| May 10, 2018 | Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, pyruvate, Model Number 11995115. Tissue and cell culture medium.Class II · It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. | Device recalls |
| Jun 22, 2017 | Ion PGM Dx SystemK170299 · PFF | 510(k) clearances |
| Mar 8, 2013 | QUANTSTUDIO DX REAL-TIME PCR INSTRUMENTK123955 · OOI | 510(k) clearances |
| Jun 21, 2012 | OPTMIZER CTS T-CELL EXPANSION SERUM FREE MEDIUMK113566 · NDS | 510(k) clearances |
| Feb 18, 2011 | STEMPRO MSC SFMK103302 · NDS | 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
