510(k) Report

FDA applicant

Hoogland Spine Products, GmbH

Muenchen, DE3 decisions2009–20220 recalls

FDA records 3 decisions for Hoogland Spine Products, GmbH (Muenchen, DE) from 2009 to 2022: 3 510(k) clearances. Most are in product codes HRX (Arthroscope) and GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 7 predicates, 0 of them its own earlier devices. No 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 Hoogland Spine Products, GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2009: 22022: 1
2009high 2 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Hoogland Spine Products, GmbH by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Which product codes does it file in?

  • HRXArthroscope2decisions
  • GEIElectrosurgical, Cutting & Coagulation & Accessories1decision

Whose devices does it build on?

Its devices cite 7 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 0 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.

  • K083552Maxmorespine Tom StickHoogland Spine Products, GmbH · 20092cite it
  • K090132Maxmorespine Spinal SystemHoogland Spine Products, GmbH · 20091cites it

What has FDA decided for it lately?

  • K211173maxmorespine Bipolar ElectrodesHoogland Spine Products, GmbH · 2022
  • K083552Maxmorespine Tom StickHoogland Spine Products, GmbH · 2009
  • K090132Maxmorespine Spinal SystemHoogland Spine Products, GmbH · 2009

All 3 as Hoogland Spine Products, GmbH →