FDA applicant

Patton, Boggs & Blow

Washington, DC6 decisions1983–19940 recalls

FDA records 6 decisions for Patton, Boggs & Blow (Washington, DC) from 1983 to 1994: 6 510(k) clearances. Most are in product codes JEY (Plate, Bone) and CDM (Diazonium Colorimetry, Urobilinogen (Urinary…). 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, dental panel, where it files most

How often FDA has decided Patton, Boggs & Blow’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Patton, Boggs & Blow since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Patton, Boggs & Blow by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Patton”

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

Patton Medical Corp. 4 Patton Surgical Corp. 2 Patton Medical Devices 1 Patton Machine Co. 1

Patton, Boggs & Blow

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Patton”