Pilling Co.
Fort Washington, PA, US
Pilling Co. appears in FDA device records in Fort Washington, PA. FDA records list 40 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 40
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 40 510(k) clearances for Pilling Co. between 1976 and 2000. The busiest year on record is 1976, with 11. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 11 |
| 1977 | 5 |
| 1980 | 1 |
| 1983 | 1 |
| 1985 | 1 |
| 1986 | 8 |
| 1987 | 2 |
| 1988 | 1 |
| 1989 | 1 |
| 1991 | 4 |
| 1992 | 1 |
| 1993 | 2 |
| 1994 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K002582 | PILLING E-FRAZIER BIPOLAR SUCTION TUBE | GEI | Substantially Equivalent | |
| K934427 | PILLING LAPAROSCOPIC INSTRUMENTATION | GEI | Substantially Equivalent | |
| K925370 | TRIANGULAR JAW MICROLARYNGEAL FORCEPS | ELW | Substantially Equivalent | |
| K925198 | KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR | GCJ | Substantially Equivalent | |
| K922971 | NO-SCALPEL VASCETOMY INSTRUMENTS | KOA | Substantially Equivalent | |
| K914015 | CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP | GBZ | Substantially Equivalent | |
| K911099 | MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE | DWX | Substantially Equivalent | |
| K911100 | MEHIGAN-PILLING PHLEBETOME TM | MGZ | Substantially Equivalent | |
| K904507 | PILLING BRUSH VALVULOTOME | DWQ | Substantially Equivalent | |
| K884946 | JEHLE CORONARY PERFUSION CATHETERS | KRA | Substantially Equivalent | |
| K882930 | LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX | CCW | Substantially Equivalent | |
| K874242 | JEHLE CORONARY PERFUSION CATHETERS | KRA | Substantially Equivalent | |
| K874243 | ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 | GAD | Substantially Equivalent | |
| K861922 | TITANIUM HEMOSTATIC CLIPS | FZP | Substantially Equivalent | |
| K861924 | MICRO ANASTOMOSIS CLAMP | DXC | Substantially Equivalent | |
| K861921 | LASER BRONCHOSCOPE SYSTEM | LLO | Substantially Equivalent | |
| K861923 | STERILE DISPOSABLE SUCTION TUBE CATHETER | Substantially Equivalent | ||
| K854916 | PILLING HEMOSTATIC CLIP APPLIER FORCEPS | GEN | Substantially Equivalent | |
| K854915 | PILLING DISPOSABLE AORTA PUNCH | Substantially Equivalent | ||
| K854914 | PILLING IDENTILOOPS | Substantially Equivalent | ||
| K854913 | MOBIN-VDDIN VEIN GRAFT HOLDER | Substantially Equivalent | ||
| K853678 | KAMBIN SPINAL INSTRUMENT SET | HTZ | Substantially Equivalent | |
| K832636 | FRAZIER SUCTION INSTRUMENT-DISPOS | GEA | Substantially Equivalent | |
| K800623 | JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE | KCD | Substantially Equivalent | |
| K772055 | PENTAX F.O.-IT OBSERVER SCOPE | Substantially Equivalent | ||
| K771739 | PENTAX LH-150F LIGHT SOURCE | FCW | Substantially Equivalent | |
| K770879 | BRONCHOFIBERSCOPE, FB-19A | Substantially Equivalent | ||
| K761141 | ARTERIAL GRAFT SIZERS | Substantially Equivalent | ||
| K761142 | HEADLIGHTS W/ FILTER-OPTICO CABLES | FST | Substantially Equivalent | |
| K760652 | JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S | EOX | Substantially Equivalent | |
| K761169 | GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP | DXC | Substantially Equivalent | |
| K761079 | FLEXIBLE TIP ASPIRATING TUBES | BYY | Substantially Equivalent | |
| K760654 | MULTI-PORTED FACE PLATE | Substantially Equivalent | ||
| K760653 | ADAPTER/STANDARD FIBER OPTICS LIGHT | EQH | Substantially Equivalent | |
| K760647 | ADAPTER, FIBER OPTICS HEADLIGHT | FCW | Substantially Equivalent | |
| K760353 | CRYOLYZER ALPHA | GEH | Substantially Equivalent | |
| K760648 | TIBIAL ARTERY CLAMP W/ATRAUGRIP JAWS | DWS | Substantially Equivalent | |
| K760646 | CAROTID ARTERY CLAMP W/PILLING LMM | DWS | Substantially Equivalent | |
| K760645 | CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP | DWS | Substantially Equivalent | |
| K760171 | FIBERBRONCHOSCOPE (PENTAX FB-17A) | EOQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KCDBougie, Esophageal, Ent
- EOQBronchoscope (Flexible Or Rigid)
- GEACannula, Surgical, General & Plastic Surgery
- GBZCatheter, Cholangiography
- KRACatheter, Continuous Flush
- DXCClamp, Vascular
- FZPClip, Implantable
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- EOXEsophagoscope (Flexible Or Rigid)
- GENForceps, General & Plastic Surgery
- HTZInstrument, Cutting, Orthopedic
- DWSInstruments, Surgical, Cardiovascular
- GCJLaparoscope, General & Plastic Surgery
- CCWLaryngoscope, Rigid
- LLOLaser, Neodymium:Yag, Pulmonary Surgery
- FCWLight Source, Fiberoptic, Routine
- FSTLight, Surgical, Fiberoptic
- ELWMaterial, Impression
- GADRetractor
- EQHSource, Carrier, Fiberoptic Light
- DWXStripper, Artery, Intraluminal
- DWQStripper, Vein, External
- KOASurgical Instruments, G-U, Manual (And Accessories)
- BYYTube, Aspirating, Flexible, Connecting
- GEHUnit, Cryosurgical, Accessories
- MGZValvulotome
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
