Medical device 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 Zimmer BiometLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 6 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Biomet Manufacturing with 131 510(k) clearances. The most recent is a 510(k) clearance dated Jul 25, 2023: Patient Specific Planning Solution™ 3D Bone Models.
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.
| Jul 25, 2023 | Patient Specific Planning Solution™ 3D Bone ModelsK230540 · LLZ | 510(k) clearances |
| Mar 15, 2023 | Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder SystemK214001 · PHX | 510(k) clearances |
| Nov 4, 2021 | Comprehensive® Convertible Glenoid - Vivacit-E LinerK211729 · PHX | 510(k) clearances |
| Feb 19, 2021 | Comprehensive Vault Reconstruction SystemK202232 · PHX | 510(k) clearances |
| Oct 28, 2020 | Comprehensive Shoulder SystemK193038 · MBF | 510(k) clearances |
| Apr 22, 2019 | Comprehensive Nano Stemless ShoulderK182516 · PKC | 510(k) clearances |
| Sep 24, 2018 | Comprehensive Reverse Shoulder SystemK181611 · PHX | 510(k) clearances |
| Feb 8, 2018 | Comprehensive Segmental Revision System (SRS)K173411 · PHX | 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
