Pilling Co.: FDA filings under this applicant name

FDA lists 40 510(k) clearances under 2 spellings of the applicant name “Pilling Co.” (first 1976, latest 2000), across 27 product codes in 7 review panels. Median 510(k) review time under this name: 46 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
DWSInstruments, Surgical, Cardiovascular33
DXCClamp, Vascular22
FCWLight Source, Fiberoptic, Routine22
GEIElectrosurgical, Cutting & Coagulation & Accessories22
KRACatheter, Continuous Flush22
BYYTube, Aspirating, Flexible, Connecting11
CCWLaryngoscope, Rigid11
DWQStripper, Vein, External11
DWXStripper, Artery, Intraluminal11
ELWMaterial, Impression11

Plus 17 more product codes.

Review panels

Most recent Pilling Co. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K002582PILLING E-FRAZIER BIPOLAR SUCTION TUBEGEI2000-11-0377
K934427PILLING LAPAROSCOPIC INSTRUMENTATIONGEI1994-01-10122
K925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSELW1993-03-18146
K925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRGCJ1993-02-12119
K922971NO-SCALPEL VASCETOMY INSTRUMENTSKOA1992-09-2396
K914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPGBZ1991-11-2173
K911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINEDWX1991-06-25105
K911100MEHIGAN-PILLING PHLEBETOME TMMGZ1991-06-21101
K904507PILLING BRUSH VALVULOTOMEDWQ1991-03-01150
K884946JEHLE CORONARY PERFUSION CATHETERSKRA1989-02-0670

30 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Pilling Co..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

FDA spellings included

FDA records this applicant under 2 spellings (case, punctuation and legal-suffix variants of one name); this page adds them up. Filings per spelling:

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Pilling Co.?

FDA lists 40 510(k) clearances under 2 spellings of the applicant name “Pilling Co.” (first 1976, latest 2000), across 27 product codes in 7 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Pilling Co.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Pilling Co. is 46 days.

Which FDA product codes appear under Pilling Co.?

The most frequent FDA product codes under this applicant name are DWS (Instruments, Surgical, Cardiovascular, 3); DXC (Clamp, Vascular, 2); FCW (Light Source, Fiberoptic, Routine, 2).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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