Vive SUP1060S

by Vive Health LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00818323021035 UDI-DI	Date8 Nov 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Vive
Generic name: Compression/pressure glove
Model / reference: SUP1060S

Primary DI / UDI-DI: 00818323021035
FDA product code: MHW
GMDN term: Compression/pressure glove

Device class: Class I
Regulation number: 880.5075
GUDID distribution status: In Commercial Distribution

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Class I

See all devices from Vive Health LLC →

Properties

Over-the-counter
Premarket exempt

Other properties (13)

Supplied sterile: No
Sterilise before use: No
Single use: No
Implantable: No
Contains latex: No
Prescription use: No
Convenience kit: No
Combination product: No
HCT/P: No
Lot / batch number: No
Serial number: No
Expiration date: No
Manufacturing date: No