Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ld Technology, LLC — Predicate Candidate Screening
14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
97 daysmedian FDA review time
168 days90th percentile
14clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K200287 | BP-BT Kiosk | Ld Technology, LLC | 2020-05-15 | 100 | 0 |
| K200141 | Oxi-W System | Ld Technology, LLC | 2020-04-27 | 97 | 0 |
| K173696 | TBL-ABI System | Ld Technology, LLC | 2017-12-19 | 18 | 0 |
| K160956 | LD-Oxi system | Ld Technology, LLC | 2016-07-06 | 92 | 0 |
| K152216 | SudoC | Ld Technology, LLC | 2015-09-24 | 48 | 0 |
| K143152 | TM-ABI system | Ld Technology, LLC | 2015-07-22 | 261 | 0 |
| K140412 | ANS1 SOFTWARE | Ld Technology, LLC | 2014-05-22 | 93 | 0 |
| K131568 | SUDO PATH | Ld Technology, LLC | 2013-06-28 | 29 | 0 |
| K130056 | PATIENT MONITOR | Ld Technology, LLC | 2013-04-11 | 92 | 0 |
| K113264 | ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) | Ld Technology, LLC | 2012-03-02 | 119 | 0 |
| K103026 | ELECTRO SENSOR -BODY COMPOSITION | Ld Technology, LLC | 2011-03-29 | 168 | 0 |
| K102166 | ELECTRO INTERSTITIAL SCAN | Ld Technology, LLC | 2010-12-10 | 130 | 0 |
| K102442 | E.S.O. (ELECTRO SENSOR OXI) | Ld Technology, LLC | 2010-09-10 | 15 | 0 |
| K083229 | E.S TECK ( ELECTRO SENSOR TECK) | Ld Technology, LLC | 2009-02-23 | 112 | 0 |
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