Mego Afek AC , Ltd.: FDA filings under this applicant name

FDA lists 17 510(k) clearances under the applicant name “Mego Afek AC , Ltd.” (first 2008, latest 2022), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 90 days. Since 2017 the median was 89 days, against 132 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
20121106
20131169
2014390
20151111
20160—
2017389
20180—
2019381
20200—
20210—
20221108
20230—
20240—
20250—
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Mego Afek AC , Ltd. took a median 89 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 132 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
JOWSleeve, Limb, Compressible1111
IRPMassager, Powered Inflatable Tube66

Review panels

Most recent Mego Afek AC , Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K214053Amputee Garment for use with Lympha Press Optimal PlusJOW2022-04-14108
K190493Recovery Pump, 737R (RPX)IRP2019-05-1576
K190015Ballancer Gold, 1212IRP2019-03-2581
K182003Lympha Press Optimal PlusJOW2019-02-27216
K172277Phlebo Press DVT ModelJOW2017-11-0398
K170658Lympha Press Optimal PlusJOW2017-05-3189
K163280RP Lite 760RIRP2017-01-2767
K150269Ballancer 505 System, Model 1201-ACIRP2015-05-26111
K142772Phlebo Press DVT 603JOW2014-12-1682
K140519RECOVERY PUMP 737RIRP2014-06-16108

7 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Mego Afek AC , Ltd..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Mego Afek AC , Ltd.?

FDA lists 17 510(k) clearances under the applicant name “Mego Afek AC , Ltd.” (first 2008, latest 2022), across 2 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Mego Afek AC , Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Mego Afek AC , Ltd. is 90 days. Since 2017: 89 days, versus 132 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Mego Afek AC , Ltd.?

The most frequent FDA product codes under this applicant name are JOW (Sleeve, Limb, Compressible, 11); IRP (Massager, Powered Inflatable Tube, 6).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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