FDA applicant

Little Doctor Electronic (Nantong)Co.,Ltd

Nantong, CN3 decisions2013–20200 recalls

FDA records 3 decisions for Little Doctor Electronic (Nantong)Co.,Ltd (Nantong, CN) from 2013 to 2020: 3 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DXQ (Blood Pressure Cuff). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Little Doctor Electronic (Nantong)Co.,Ltd’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2013high 2 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Little Doctor Electronic (Nantong)Co.,Ltd by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Little Doctor Electronic…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Little”

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

Little Nell Labs, Inc. 1 Little Doctor (Shanghai) Electronic Manufacturing 1 Little Sparrows Technologies, Inc. 1 Little Doctor (Shanghai) Electronic 1 Little Rapids Corporation 1

Little Doctor Electronic (Nantong)Co.,Ltd

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Little”