Mag & More GmbH: FDA clearances and approvals

Mag & More GmbH has 5 FDA 510(k) clearances (first 2018, latest 2026), across 1 product code in 1 review panel. Median 510(k) review time: 268 days. Since 2017 its median was 268 days, against 137 days for all cleared 510(k)s in the same product codes.

510(k) clearances per year

YearClearancesMedian review days
2018188
20190—
20200—
20210—
20220—
20230—
20241268
20252278
2026192

Review time against the same product codes

Since 2017, Mag & More GmbH's cleared 510(k)s took a median 268 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 137 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
OBPTranscranial Magnetic Stimulator55

Review panels

Most recent Mag & More GmbH 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K260560Apollo TMS Therapy System;Apollo light TMS Therapy SystemOBP2026-05-2292
K243700Apollo TMS Therapy SystemOBP2025-09-04279
K243539Apollo TMS Therapy SystemOBP2025-08-18276
K232639Apollo TMS Therapy SystemOBP2024-05-24268
K180313Apollo TMS Therapy SystemOBP2018-05-0488

Recalls

openFDA lists no recalls under a recalling firm named Mag & More GmbH.

Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.

Frequently asked questions

How many FDA 510(k) clearances does Mag & More GmbH have?

Mag & More GmbH has 5 FDA 510(k) clearances (first 2018, latest 2026), across 1 product code in 1 review panel.

How long does FDA take to clear Mag & More GmbH's 510(k)s?

The median time from FDA receipt to decision across Mag & More GmbH's cleared 510(k)s is 268 days. Since 2017: 268 days, versus 137 days for all cleared 510(k)s in the same product codes.

What devices does Mag & More GmbH make?

Its most frequent FDA product codes are OBP (Transcranial Magnetic Stimulator, 5).

Has Mag & More GmbH had device recalls?

openFDA lists no recalls under a recalling firm name matching Mag & More GmbH. Related entities may recall under other names.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.

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