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Data / Medical devices / Tracking, Soft Tissue, Intraoperative

Tracking, Soft Tissue, Intraoperative (OEW): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Tracking, Soft Tissue, Intraoperative (product code OEW, Class 2, 21 CFR 882.4560). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on April 28, 2015, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
OEW
Device class
2
Regulation
882.4560
Medical specialty
Neurology
Life sustaining or supporting
Yes

Makers by country

CountryMakers
United States2
Switzerland1
China1

Makers of Tracking, Soft Tissue, Intraoperative

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CascinationBern, SwitzerlandManufacturer1April 28, 2015000api.fda.gov
ATL Technology DG,Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Hologic, Inc.Marlborough, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Hologic, Inc.Marlborough, MA, United StatesManufacturer0000api.fda.gov

Updated April 28, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.