FirmLabelled by claude-haiku-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 FH Industrie with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 9, 2026: JARVIS Metaphyseal Stem.
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.
| Jan 9, 2026 | JARVIS Metaphyseal StemK254003 · PHX | 510(k) clearances |
| Oct 29, 2025 | JARVIS Diaphyseal Stem StandardK253345 · PHX | 510(k) clearances |
| Aug 28, 2025 | JARVIS Glenoid Reverse Shoulder ProsthesisK252411 · PHX | 510(k) clearances |
| Nov 25, 2024 | JARVIS Glenoid Reverse Shoulder ProsthesisK242253 · PHX | 510(k) clearances |
| Aug 29, 2023 | ARROW Off-Centred Humeral InsertK232226 · PHX | 510(k) clearances |
| Sep 30, 2022 | e-Ortho Shoulder Software v1.1K220758 · LLZ | 510(k) clearances |
| Nov 30, 2021 | ARROW Short Stem Humeral SystemK202024 · PHX | 510(k) clearances |
| Oct 1, 2020 | TELEGRAPH® EVOLUTION Humeral Nailing SystemK200127 · HSB | 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
