Shenzhen Osto Technology Company Limited: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Shenzhen Osto Technology Company Limited” (first 2014, latest 2022), across 3 product codes in 3 review panels. Median 510(k) review time under this name: 272 days. Since 2017 the median was 222 days, against 140 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
20141324
20150—
20160—
20170—
20180—
20191272
20201353
2021390
20221288
20230—
20240—
20250—
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Shenzhen Osto Technology Company Limited took a median 222 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 140 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
NUHStimulator, Nerve, Transcutaneous, Over-The-Counter55
NGXStimulator, Muscle, Powered, For Muscle Conditioning11
OLPOver-The-Counter Powered Light Based Laser For Acne11

Review panels

Most recent Shenzhen Osto Technology Company Limited 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K213056LED Facial MaskOLP2022-07-07288
K211942Heating Lumbar Therapy Cushion (Model: AST-622, AST-622B, AST-623, AST-623B)NGX2021-12-13173
K211736Electronic Muscle Stimulator (Model: AST-300A, AST-300N, AST-300S, AST-300T, AST-300V, AST-300W)NUH2021-09-0590
K210756Neck Care Therapy, Model: AST-905A, AST-905D, AST-905HNUH2021-06-1188
K190783Health Expert Electronic Stimulator (model: AST-300L)NUH2020-03-14353
K190673Health Expert Electronic StimulatorNUH2019-12-12272
K133929HEALTH EXPERT ELCTRONIC STIMULATORNUH2014-11-12324

Recalls

openFDA lists no recalls under a recalling firm named Shenzhen Osto Technology Company Limited.

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 Shenzhen Osto Technology Company Limited?

FDA lists 7 510(k) clearances under the applicant name “Shenzhen Osto Technology Company Limited” (first 2014, latest 2022), across 3 product codes in 3 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 Shenzhen Osto Technology Company Limited?

The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Osto Technology Company Limited is 272 days. Since 2017: 222 days, versus 140 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Shenzhen Osto Technology Company Limited?

The most frequent FDA product codes under this applicant name are NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter, 5); NGX (Stimulator, Muscle, Powered, For Muscle Conditioning, 1); OLP (Over-The-Counter Powered Light Based Laser For Acne, 1).

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, with punctuation and legal suffixes removed; 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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