FDA applicant

Hogan Lovells US LLP

Philedelphia, PA3 decisions2012–20140 recalls

FDA records 3 decisions for Hogan Lovells US LLP (Philedelphia, PA) from 2012 to 2014: 3 510(k) clearances. Most are in product codes NKB (Thoracolumbosacral Pedicle Screw System) and OWI (Bone Fixation Cerclage, Sublaminar). Its devices cite 4 predicates, 0 of them its own earlier devices. 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, orthopedic panel, where it files most

How often FDA has decided Hogan Lovells US LLP’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2012high 1 (2012) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Hogan Lovells US LLP by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hogan Lovells US LLP’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 “Hogan”

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

Hogan & Hartson 26 Hogan/Cologne Ent. 1

Hogan Lovells US LLP

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Hogan”