FDA applicant

Baumer Ortopedia, Ltd.

Mogi Mirim-Sp-Brasil, BR5 decisions1994–19940 recalls

FDA records 5 decisions for Baumer Ortopedia, Ltd. (Mogi Mirim-Sp-Brasil, BR) in 1994: 5 510(k) clearances. Most are in product codes HTY (Pin, Fixation, Smooth) and HWC (Screw, Fixation, Bone). 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 Baumer Ortopedia, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Baumer Ortopedia, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Baumer”

FDA records each applicant name separately; these may or may not be the same firm.

Baumer, S.A 4

Baumer Ortopedia, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Baumer”