510(k) Report

FDA applicant

Narang Medical, Ltd.

Delhi, IN2 decisions2015–20240 recalls

FDA records 2 decisions for Narang Medical, Ltd. (Delhi, IN) from 2015 to 2024: 2 510(k) clearances. Most are in product codes JDS (Nail, Fixation, Bone) and HRS (Plate, Fixation, Bone). Its devices cite 23 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Narang Medical Limited”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Narang Medical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2015: 12024: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Narang Medical, Ltd. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Narang”

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