Zhejiang Longterm Medical Technology Co., Ltd.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Zhejiang Longterm Medical Technology Co., Ltd.” (first 2019, latest 2026), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 281 days. Since 2017 the median was 281 days, against 233 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
20191255
20201281
20211447
20221375
20230—
20240—
20250—
20261255

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Zhejiang Longterm Medical Technology Co., Ltd. took a median 281 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 233 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
OMPNegative Pressure Wound Therapy Powered Suction Pump33
FRODressing, Wound, Drug11
NADDressing, Wound, Occlusive11

Review panels

Most recent Zhejiang Longterm Medical Technology Co., Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K254246LT Antibacterial Foam with Silver DressingNAD2026-09-10255
K211571Small Foam Kit, Medium Foam Kit, Large Foam Kit, Extra Large Foam KitOMP2022-05-31375
K202823Innomed NPWT Silicone Foam DressingOMP2021-12-15447
K192478LT Antibacterial Alginate with Silver DressingFRO2020-06-17281
K182458Longterm NPWT Foam Dressing KitOMP2019-05-23255

Recalls

openFDA lists no recalls under a recalling firm named Zhejiang Longterm Medical Technology Co., 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 Zhejiang Longterm Medical Technology Co., Ltd.?

FDA lists 5 510(k) clearances under the applicant name “Zhejiang Longterm Medical Technology Co., Ltd.” (first 2019, latest 2026), across 3 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Zhejiang Longterm Medical Technology Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Zhejiang Longterm Medical Technology Co., Ltd. is 281 days. Since 2017: 281 days, versus 233 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Zhejiang Longterm Medical Technology Co., Ltd.?

The most frequent FDA product codes under this applicant name are OMP (Negative Pressure Wound Therapy Powered Suction Pump, 3); FRO (Dressing, Wound, Drug, 1); NAD (Dressing, Wound, Occlusive, 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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