FDA applicant

Synectics Medical, Inc.

S-116 28 Stockholm, SE5 decisions1994–19970 recalls

FDA records 5 decisions for Synectics Medical, Inc. (S-116 28 Stockholm, SE) from 1994 to 1997: 5 510(k) clearances. Most are in product codes FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic…) and BZG (Spirometer, Diagnostic). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Synectics Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Synectics Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Synectics”

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

Synectics-Dantec 19 Synectics AB 1

Synectics Medical, Inc.

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 “Synectics”