FDA applicant

Paul B. Elder Co.

Mchenry, IL3 decisions1979–19810 recalls

FDA records 3 decisions for Paul B. Elder Co. (Mchenry, IL) from 1979 to 1981: 3 510(k) clearances. All are in product code KGL (Cabinet, Phototherapy (Puva)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Paul B. Elder Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paul B. Elder Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Paul B. Elder Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Paul B. Elder Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Paul”

FDA records each applicant name separately; these may or may not be the same firm.

Paul Hartmann Corp. 5 Paul B. Heller, D.M.D. 1 Paul E. Jaffe, D.M.D. 1 Paul H. Schneider Ent. 1 Paul Weiser Co. 1 Paul Ritzau Pari GmbH 1 Paul S. Barclay, D.D.S., Ltd. 1 Paul Ritzau Pari-Werk GmbH 1

Paul B. Elder Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paul”