FDA applicant

Paul Hartmann Corp.

Greenwood, SC5 decisions1984–19840 recalls

FDA records 5 decisions for Paul Hartmann Corp. (Greenwood, SC) in 1984: 5 510(k) clearances. Most are in product codes EYQ (Garment, Protective, For Incontinence) and HHD (Pad, Menstrual, Unscented). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Paul Hartmann Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paul Hartmann Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Paul”

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

Paul B. Elder Co. 3 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 Hartmann Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paul”