Atlas FDA

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-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K934427PILLING LAPAROSCOPIC INSTRUMENTATIONPilling Co.1994-01-101220
K925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSPilling Co.1993-03-181460
K925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRPilling Co.1993-02-121190
K922971NO-SCALPEL VASCETOMY INSTRUMENTSPilling Co.1992-09-23960
K914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPPilling Co.1991-11-21730
K911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINEPilling Co.1991-06-251050
K911100MEHIGAN-PILLING PHLEBETOME TMPilling Co.1991-06-211010
K904507PILLING BRUSH VALVULOTOMEPilling Co.1991-03-011500
K884946JEHLE CORONARY PERFUSION CATHETERSPilling Co.1989-02-06700
K882930LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EXPilling Co.1988-08-16340
K874242JEHLE CORONARY PERFUSION CATHETERSPilling Co.1987-12-07520
K874243ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000Pilling Co.1987-11-13280
K861922TITANIUM HEMOSTATIC CLIPSPilling Co.1986-06-13250
K861924MICRO ANASTOMOSIS CLAMPPilling Co.1986-06-06180
K861921LASER BRONCHOSCOPE SYSTEMPilling Co.1986-06-02140
K861923STERILE DISPOSABLE SUCTION TUBE CATHETERPilling Co.1986-05-30110
K854914PILLING IDENTILOOPSPilling Co.1986-01-24460
K854913MOBIN-VDDIN VEIN GRAFT HOLDERPilling Co.1986-01-24460
K854916PILLING HEMOSTATIC CLIP APPLIER FORCEPSPilling Co.1986-01-24460
K854915PILLING DISPOSABLE AORTA PUNCHPilling Co.1986-01-24460
K853678KAMBIN SPINAL INSTRUMENT SETPilling Co.1985-09-24210
K832636FRAZIER SUCTION INSTRUMENT-DISPOSPilling Co.1983-10-14710
K800623JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUEPilling Co.1980-04-24360
K772055PENTAX F.O.-IT OBSERVER SCOPEPilling Co.1977-11-15150
K771739PENTAX LH-150F LIGHT SOURCEPilling Co.1977-09-30150
K770879BRONCHOFIBERSCOPE, FB-19APilling Co.1977-05-2590
K761141ARTERIAL GRAFT SIZERSPilling Co.1977-01-06410
K761142HEADLIGHTS W/ FILTER-OPTICO CABLESPilling Co.1977-01-05400
K760652JESBERG ESOPHAGOSCOPES W/AUSTINETIC S SPilling Co.1976-12-16920
K761169GRANT MODIF OF DEBAKEY ABDOM AORTA CLMPPilling Co.1976-12-0980
K761079FLEXIBLE TIP ASPIRATING TUBESPilling Co.1976-12-09200
K760653ADAPTER/STANDARD FIBER OPTICS LIGHTPilling Co.1976-12-06810
K760647ADAPTER, FIBER OPTICS HEADLIGHTPilling Co.1976-12-06820
K760654MULTI-PORTED FACE PLATEPilling Co.1976-12-06810
K760353CRYOLYZER ALPHAPilling Co.1976-10-29880
K760648TIBIAL ARTERY CLAMP W/ATRAUGRIP JAWSPilling Co.1976-09-2160
K760645CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMPPilling Co.1976-09-2160
K760646CAROTID ARTERY CLAMP W/PILLING LMMPilling Co.1976-09-2160
K760171FIBERBRONCHOSCOPE (PENTAX FB-17A)Pilling Co.1976-07-19130

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