510(k) Report

FDA applicant

Memometal Technologies

Bruz, FR10 decisions2007–20111 recall

FDA records 10 decisions for Memometal Technologies (Bruz, FR) from 2007 to 2011: 10 510(k) clearances. Most are in product codes HTY (Pin, Fixation, Smooth) and HWC (Screw, Fixation, Bone). Its devices cite 24 predicates, 1 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Memometal Technologies’s devices, and how often a recall has named them.

FDA decisions per year

2in 2011

2007: 52009: 12010: 22011: 2
2007high 5 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Memometal Technologies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Memometal Technologies’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • HTYPin, Fixation, Smooth3decisions
  • HWCScrew, Fixation, Bone3decisions
  • JDRStaple, Fixation, Bone2decisions
  • HRSPlate, Fixation, Bone2decisions

Whose devices does it build on?

Its devices cite 24 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 54 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K070598Memometal Intra-Medullary Bone Fastener, Models Smart Toe / X-FuseMemometal Technologies · 200714cite it
  • K070031Memometal Memory StaplesMemometal Technologies · 200713cite it
  • K083447Memometal Anchorage Bone Plate System, Models PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50Memometal Technologies · 200910cite it
  • K070039Memometal Fixos ScrewsMemometal Technologies · 20076cite it
  • K112197Memometal Intra-Medullary Bone FastenerMemometal Technologies · 20114cite it
  • K070033Memometal Varisation, Models AV26-08, AV26-10, AV90-08 and AV90-10Memometal Technologies · 20073cite it

What has FDA decided for it lately?

  • K112197Memometal Intra-Medullary Bone FastenerMemometal Technologies · 20111 recall
  • K101930Memometal Navis Bone Plating SystemMemometal Technologies · 2011
  • K102072Memometal Implants (K-Snap & TI-Fuse)Memometal Technologies · 2010
  • K093820Subfix Arthroereisis Implant, Models SUT0065, SUT0080, SUT0090, SUT0100, SUT0115Memometal Technologies · 2010
  • K083447Memometal Anchorage Bone Plate System, Models PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50Memometal Technologies · 2009
  • K071941Memometal Bone AnchorsMemometal Technologies · 2007
  • K070598Memometal Intra-Medullary Bone Fastener, Models Smart Toe / X-FuseMemometal Technologies · 2007
  • K070039Memometal Fixos ScrewsMemometal Technologies · 2007

All 10 as Memometal Technologies →

What has been recalled?

1 recall linked to its devices; the latest:

  • K112197Smart Toe II Intramedullary Arthrodesis ImplantMar 28, 2022Class II