FDA applicant

Solos Endoscopy, Inc.

Norcross, GA21 decisions1990–19980 recalls

FDA records 21 decisions for Solos Endoscopy, Inc. (Norcross, GA) from 1990 to 1998: 21 510(k) clearances. Most are in product codes FBM (Cannula And Trocar, Suprapubic, Non-Disposable) and GEN (Forceps, General & Plastic Surgery). Its devices cite 3 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, general and plastic surgery panel, where it files most

How often FDA has decided Solos Endoscopy, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Solos Endoscopy, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Solos Endoscopy, Inc.’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 “Solos”

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

Solos Ophthalmology 5 Solos Mfg. 1

Solos Endoscopy, Inc.

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 “Solos”