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Data / Medical devices / United Kingdom / Bodywise (uk) Ltd.

Bodywise (uk) Ltd.: FDA-registered device maker in BRISTOL Gloucestershire, United Kingdom, 2 510(k) clearances

Bodywise (uk) Ltd. is registered with the FDA (registration 8043647) in BRISTOL Gloucestershire, United Kingdom. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 25, 1996. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
8043647
FEI number
1000184034
Address
Natracare House 19 Eagles Wood Woodlands Lane, BRISTOL Gloucestershire, United Kingdom, BS32 4EU
Owner or operator
BODYWISE (UK) LTD. (9002921)
Roles
Manufacturer
First device listed
December 16, 1993
Registered through
2026
Brand names listed
NATRACARE

Devices it lists

DeviceProduct codeClassRoleSource
Pad, Menstrual, UnscentedHHD1Manufactureraccessdata.fda.gov
Tampon, Menstrual, UnscentedHEB2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 25, 1996K954942NATRACAREN APPLICATOR TAMPONHEBSubstantially EquivalentBodywise (Uk), Ltd.accessdata.fda.gov
September 3, 1993K914430NATRACARE TAMPONHEBSubstantially EquivalentBodywise (Uk), Ltd.accessdata.fda.gov

Compare with other makers

Updated January 25, 1996. 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.