FDA applicant

Asap Endoscopic Products GmbH

Luebeck, DE5 decisions2003–20130 recalls

FDA records 5 decisions for Asap Endoscopic Products GmbH (Luebeck, DE) from 2003 to 2013: 5 510(k) clearances. Most are in product codes HRX (Arthroscope) and FAJ (Cystoscope And Accessories, Flexible/Rigid). Its devices cite 10 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 Asap Endoscopic Products GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Asap Endoscopic Products GmbH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Asap Endoscopic Products GmbH’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 “Asap”

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

Asap Dental Lab, Ltd. 1

Asap Endoscopic Products GmbH

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 “Asap”