Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Pilling Co. — Predicate Candidate Screening
39 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
46 daysmedian FDA review time
119 days90th percentile
39clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K934427 | PILLING LAPAROSCOPIC INSTRUMENTATION | Pilling Co. | 1994-01-10 | 122 | 0 |
| K925370 | TRIANGULAR JAW MICROLARYNGEAL FORCEPS | Pilling Co. | 1993-03-18 | 146 | 0 |
| K925198 | KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR | Pilling Co. | 1993-02-12 | 119 | 0 |
| K922971 | NO-SCALPEL VASCETOMY INSTRUMENTS | Pilling Co. | 1992-09-23 | 96 | 0 |
| K914015 | CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP | Pilling Co. | 1991-11-21 | 73 | 0 |
| K911099 | MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE | Pilling Co. | 1991-06-25 | 105 | 0 |
| K911100 | MEHIGAN-PILLING PHLEBETOME TM | Pilling Co. | 1991-06-21 | 101 | 0 |
| K904507 | PILLING BRUSH VALVULOTOME | Pilling Co. | 1991-03-01 | 150 | 0 |
| K884946 | JEHLE CORONARY PERFUSION CATHETERS | Pilling Co. | 1989-02-06 | 70 | 0 |
| K882930 | LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX | Pilling Co. | 1988-08-16 | 34 | 0 |
| K874242 | JEHLE CORONARY PERFUSION CATHETERS | Pilling Co. | 1987-12-07 | 52 | 0 |
| K874243 | ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 | Pilling Co. | 1987-11-13 | 28 | 0 |
| K861922 | TITANIUM HEMOSTATIC CLIPS | Pilling Co. | 1986-06-13 | 25 | 0 |
| K861924 | MICRO ANASTOMOSIS CLAMP | Pilling Co. | 1986-06-06 | 18 | 0 |
| K861921 | LASER BRONCHOSCOPE SYSTEM | Pilling Co. | 1986-06-02 | 14 | 0 |
| K861923 | STERILE DISPOSABLE SUCTION TUBE CATHETER | Pilling Co. | 1986-05-30 | 11 | 0 |
| K854914 | PILLING IDENTILOOPS | Pilling Co. | 1986-01-24 | 46 | 0 |
| K854913 | MOBIN-VDDIN VEIN GRAFT HOLDER | Pilling Co. | 1986-01-24 | 46 | 0 |
| K854916 | PILLING HEMOSTATIC CLIP APPLIER FORCEPS | Pilling Co. | 1986-01-24 | 46 | 0 |
| K854915 | PILLING DISPOSABLE AORTA PUNCH | Pilling Co. | 1986-01-24 | 46 | 0 |
| K853678 | KAMBIN SPINAL INSTRUMENT SET | Pilling Co. | 1985-09-24 | 21 | 0 |
| K832636 | FRAZIER SUCTION INSTRUMENT-DISPOS | Pilling Co. | 1983-10-14 | 71 | 0 |
| K800623 | JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE | Pilling Co. | 1980-04-24 | 36 | 0 |
| K772055 | PENTAX F.O.-IT OBSERVER SCOPE | Pilling Co. | 1977-11-15 | 15 | 0 |
| K771739 | PENTAX LH-150F LIGHT SOURCE | Pilling Co. | 1977-09-30 | 15 | 0 |
| K770879 | BRONCHOFIBERSCOPE, FB-19A | Pilling Co. | 1977-05-25 | 9 | 0 |
| K761141 | ARTERIAL GRAFT SIZERS | Pilling Co. | 1977-01-06 | 41 | 0 |
| K761142 | HEADLIGHTS W/ FILTER-OPTICO CABLES | Pilling Co. | 1977-01-05 | 40 | 0 |
| K760652 | JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S | Pilling Co. | 1976-12-16 | 92 | 0 |
| K761169 | GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP | Pilling Co. | 1976-12-09 | 8 | 0 |
| K761079 | FLEXIBLE TIP ASPIRATING TUBES | Pilling Co. | 1976-12-09 | 20 | 0 |
| K760653 | ADAPTER/STANDARD FIBER OPTICS LIGHT | Pilling Co. | 1976-12-06 | 81 | 0 |
| K760647 | ADAPTER, FIBER OPTICS HEADLIGHT | Pilling Co. | 1976-12-06 | 82 | 0 |
| K760654 | MULTI-PORTED FACE PLATE | Pilling Co. | 1976-12-06 | 81 | 0 |
| K760353 | CRYOLYZER ALPHA | Pilling Co. | 1976-10-29 | 88 | 0 |
| K760648 | TIBIAL ARTERY CLAMP W/ATRAUGRIP JAWS | Pilling Co. | 1976-09-21 | 6 | 0 |
| K760645 | CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP | Pilling Co. | 1976-09-21 | 6 | 0 |
| K760646 | CAROTID ARTERY CLAMP W/PILLING LMM | Pilling Co. | 1976-09-21 | 6 | 0 |
| K760171 | FIBERBRONCHOSCOPE (PENTAX FB-17A) | Pilling Co. | 1976-07-19 | 13 | 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