Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Li Medical Technologies, Inc. — Predicate Candidate Screening
17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
78 daysmedian FDA review time
212 days90th percentile
17clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K002413 | ULTRASORB SUTURE ANCHOR | Li Medical Technologies, Inc. | 2000-09-19 | 43 | 0 |
| K993373 | ROTORBLADE SUTURE ANCHOR | Li Medical Technologies, Inc. | 1999-10-27 | 20 | 0 |
| K992938 | ROTORBLADE SUTURE ANCHOR | Li Medical Technologies, Inc. | 1999-09-23 | 23 | 0 |
| K983435 | ROTORBLADE | Li Medical Technologies, Inc. | 1999-04-29 | 212 | 0 |
| K981764 | LM ANCHOR | Li Medical Technologies, Inc. | 1998-07-13 | 55 | 0 |
| K981755 | LM ANCHOR | Li Medical Technologies, Inc. | 1998-07-13 | 56 | 0 |
| K963288 | LM BONE ANCHOR | Li Medical Technologies, Inc. | 1996-11-13 | 84 | 0 |
| K963812 | LM BONE ANCHOR (ORTHOPEDICS) | Li Medical Technologies, Inc. | 1996-11-12 | 64 | 0 |
| K960825 | LM ANCHOR OR OTHER PROPRIETARY NAME | Li Medical Technologies, Inc. | 1996-04-30 | 61 | 0 |
| K960439 | LM BONE ANCHOR | Li Medical Technologies, Inc. | 1996-04-18 | 78 | 0 |
| K960448 | LM ANCHOR | Li Medical Technologies, Inc. | 1996-04-17 | 78 | 0 |
| K953764 | LMT BONE ANCHOR | Li Medical Technologies, Inc. | 1995-08-25 | 14 | 0 |
| K951233 | LMT BONE ANCHOR | Li Medical Technologies, Inc. | 1995-07-03 | 105 | 0 |
| K951472 | LMT BONE ANCHOR | Li Medical Technologies, Inc. | 1995-07-03 | 95 | 0 |
| K941964 | LMT ARTHROSCOPIC SUTURING INSTRUMENTS | Li Medical Technologies, Inc. | 1994-09-28 | 159 | 0 |
| K933025 | LAPORASCOPIC CANNULA SEAL | Li Medical Technologies, Inc. | 1994-01-25 | 217 | 0 |
| K931142 | INSTRUMENTS FOR LAPAROSCOPIC USE | Li Medical Technologies, Inc. | 1993-06-25 | 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