Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FranceLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of StrykerLabelled by claude-sonnet-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 Memometal Technologies with 10 510(k) clearances. The most recent is a 510(k) clearance dated Nov 17, 2011: MEMOMETAL INTRA-MEDULLARY BONE FASTENER.
| Nov 17, 2011 | MEMOMETAL INTRA-MEDULLARY BONE FASTENERK112197 · HTY | 510(k) clearances |
| Mar 15, 2011 | MEMOMETAL NAVIS BONE PLATING SYSTEMK101930 · HRS | 510(k) clearances |
| Nov 3, 2010 | MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)K102072 · HTY | 510(k) clearances |
| May 19, 2010 | SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115K093820 · HWC | 510(k) clearances |
| Feb 6, 2009 | MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50K083447 · HRS | 510(k) clearances |
| Dec 4, 2007 | MEMOMETAL BONE ANCHORSK071941 · HWC | 510(k) clearances |
| Jul 26, 2007 | MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSEK070598 · HTY | 510(k) clearances |
| Mar 21, 2007 | MEMOMETAL FIXOS SCREWSK070039 · HWC | 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
