FDA applicant

Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar

Ankara, TR1 decision2009–20090 recalls

FDA records 1 decision for Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar (Ankara, TR) in 2009: 1 510(k) clearance. All are in product code MNH (Orthosis, Spondylolisthesis Spinal Fixation). Its devices cite 2 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 Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Norm Tibbi Urunler Ithalat Ihracat…’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 “Norm”

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

Norm Pacific Automation Corp. 5

Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Norm”