FDA applicant

Meditech Advisors, LLC

Ashland, MA2 decisions2009–20130 recalls

FDA records 2 decisions for Meditech Advisors, LLC (Ashland, MA) from 2009 to 2013: 2 510(k) clearances. Most are in product codes ODP (Intervertebral Fusion Device With Bone Graft…) and MAX (Intervertebral Fusion Device With Bone Graft…). 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 Meditech Advisors, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Meditech Advisors, LLC by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Meditech Advisors, LLC’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 “Meditech”

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

Meditech Spine, LLC 10 Meditech International, Inc. 5 Meditech, Inc. 3 Meditech Gloves Sdn Bhd 2 Meditech Kft. 2 Meditech Endoscopy, Ltd. 1

Meditech Advisors, LLC

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 “Meditech”