FDA applicant

Eska Implants GmbH & Co.

Round Rock, TX2 decisions2003–20060 recalls

FDA records 2 decisions for Eska Implants GmbH & Co. (Round Rock, TX) from 2003 to 2006: 2 510(k) clearances. Most are in product codes LPH (Prosthesis, Hip, Semi-Constrained…) and JDI (Prosthesis, Hip, Semi-Constrained…). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Eska Implants GmbH”.

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 Eska Implants GmbH & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eska Implants GmbH & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eska Implants GmbH & Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Eska”

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

Eska America Corp. 1

Eska Implants GmbH & Co.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Eska”