Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
LRW · Predicate Candidate Screening
18 FDA 510(k) clearances under this product code; the 50 most recent screened below.
25 daysmedian FDA review time
56 days90th percentile
18clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K911158 | MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM | Northgate Technologies, Inc. | 1991-03-29 | 14 | 0 |
| K902828 | SUTURE REMOVAL TRAY | Orion Life Systems, Inc. | 1990-08-08 | 41 | 0 |
| K900950 | GS-2000 MICRO SCISSOR, CURVED LEFT, 5MM | Solos Endoscopy, Inc. | 1990-04-18 | 50 | 0 |
| K900957 | GS-2100 HOOK SUTURE SCISSOR, 5MM | Solos Endoscopy, Inc. | 1990-04-18 | 50 | 0 |
| K892823 | PLASTER CUTTING SCISSORS | The South India Surgical Co. Pvt. , Ltd. | 1989-05-25 | 44 | 0 |
| K891889 | OLIVECORONA SCISSORS | Zinnanti Surgical Instruments, Inc. | 1989-04-12 | 19 | 0 |
| K891886 | SCISSORS, VARIOUS TYPES | Zinnanti Surgical Instruments, Inc. | 1989-04-12 | 19 | 0 |
| K891200 | RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS | Zinnanti Surgical Instruments, Inc. | 1989-04-06 | 31 | 0 |
| K891203 | SCISSORS: THOREK, JORGENSEN, FINOCHIETTO | Zinnanti Surgical Instruments, Inc. | 1989-04-06 | 31 | 0 |
| K890170 | SCISSORS | Dhason Brothers, Inc. | 1989-02-03 | 25 | 0 |
| K890235 | DRESSING SCISSORS | Kinetic Medical Products | 1989-02-03 | 16 | 0 |
| K890264 | STRABISMUS SCISSORS | Kinetic Medical Products | 1989-01-27 | 9 | 0 |
| K884373 | KORBER ARTERIOTOMY SCISSORS | Micrins, Ltd. | 1988-11-08 | 21 | 0 |
| K884095 | SCISSORS, WIRE CUTTING | Magnatrade Corp. | 1988-10-19 | 21 | 0 |
| K873046 | OVONIC COATED SURGICAL SCISSORS | Micrins, Ltd. | 1987-08-26 | 22 | 0 |
| K871923 | MICRO SCISSOR, 1.7MM | Arthropedics, Inc. | 1987-06-01 | 14 | 0 |
| K851802 | 69-140 TO 69-160 VARIOUS NAIL CUTTERS | Artiberia | 1985-06-20 | 56 | 0 |
| K851801 | 69-120 TO 69-132 VARIOUS NAIL SCISSORS | Artiberia | 1985-06-20 | 56 | 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