Tillotson Rubber Co., Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Tillotson Rubber Co., Inc.” (first 1977, latest 1991), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 42 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
20120—
20130—
20140—
20150—
20160—
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
LYYLatex Patient Examination Glove33
KGOSurgeon'S Gloves22
FMLChair, Blood Donor11

Review panels

Most recent Tillotson Rubber Co., Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K905765PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)LYY1991-02-2560
K903756STERILE PATIENT EXAMINATION GLOVESLYY1990-09-0523
K903607POWDER FREE, NON-STERILE EXAMINATION GLOVESLYY1990-08-1710
K894828HPI ORTHO SURGEONS' GLOVEKGO1990-05-07280
K780181GLOVES, FLOORFML1978-02-2118
K770704GLOVES, SURGEONS, LATEXKGO1977-06-2467

Recalls

openFDA lists no recalls under a recalling firm named Tillotson Rubber Co., Inc..

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.

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 Tillotson Rubber Co., Inc.?

FDA lists 6 510(k) clearances under the applicant name “Tillotson Rubber Co., Inc.” (first 1977, latest 1991), across 3 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Tillotson Rubber Co., Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Tillotson Rubber Co., Inc. is 42 days.

Which FDA product codes appear under Tillotson Rubber Co., Inc.?

The most frequent FDA product codes under this applicant name are LYY (Latex Patient Examination Glove, 3); KGO (Surgeon'S Gloves, 2); FML (Chair, Blood Donor, 1).

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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

All FDA device companies · FDA product code lookup