Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Lg Electronics.Inc — Predicate Candidate Screening

28 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

64 daysmedian FDA review time
148 days90th percentile
28clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc2026-07-17630
K261213Medical Monitor (40HT513D)Lg Electronics.Inc2026-06-12590
K251209Medical Monitor (32HS710S)Lg Electronics.Inc2025-06-12550
K243439Medical Monitor (27HS714S)Lg Electronics.Inc2025-01-28830
K241402Medical Monitor (32HR734S)Lg Electronics.Inc2024-08-12870
K233599X-Clever (ASHK100G)Lg Electronics.Inc2024-03-181300
K240130Medical Monitor (21HQ613D)Lg Electronics.Inc2024-02-15290
K23298524HR513CLg Electronics.Inc2023-12-11800
K23212721HQ513D, 32HL512D, 31HN713D, 32HQ713DLg Electronics.Inc2023-08-15290
K23084532HL512D, 31HN713D, 32HQ713DLg Electronics.Inc2023-04-27300
K22342332HQ713DLg Electronics.Inc2023-03-011070
K22354614HQ721G-BLg Electronics.Inc2023-01-27630
K22378921HQ513DLg Electronics.Inc2023-01-09210
K22146110HQ701G-BLg Electronics.Inc2022-07-22640
K22139414HQ701G-BLg Electronics.Inc2022-07-22700
K22143417HQ701G-BLg Electronics.Inc2022-07-13570
K22106121HQ613DLg Electronics.Inc2022-06-03530
K22055917HQ901G-BLg Electronics.Inc2022-05-05660
K21404414HQ901G-BLg Electronics.Inc2022-02-16510
K212137X-CleverLg Electronics.Inc2021-12-101550
K21229521HQ513DLg Electronics.Inc2021-12-031340
K20177731HN713DLg Electronics.Inc2020-10-081010
K200464LG Pra. L Derma LD Scalp CareLg Electronics.Inc2020-07-231480
K19292532HL512DLg Electronics.Inc2020-03-131490
K19186421HK512DLg Electronics.Inc2019-12-051460
K183671LG PRA.L DERMA LED MASKLg Electronics.Inc2019-01-22260
K18328617HK701G-WLg Electronics.Inc2018-12-07110
K18234814HK701G-WLg Electronics.Inc2018-10-18500

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda