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Data / Medical devices / Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride)

Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride) (MXW): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride) (product code MXW, Class 2, 21 CFR 878.5010). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on January 17, 2007, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
MXW
Device class
2
Regulation
878.5010
Medical specialty
General, Plastic Surgery
Implant
Yes

Makers by country

CountryMakers
Germany2
Czechia1

Makers of Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride)

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
Medizin Produkte Neustadt GmbH (MPN)Neustadt in Holstein Schleswig-Holstein, GermanyManufacturer0000api.fda.gov
RESORBA Medical GmbHNUERNBERG Bavaria, GermanyManufacturer0000api.fda.gov
Resorba, s.r.oDomazlice, CzechiaManufacturer0000api.fda.gov

Updated January 17, 2007. 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.