Procare 79-91100

Procare 79-91100 is a Class I device made by Djo, LLC, listed in FDA GUDID since 12 Aug 2021 (UDI-DI 00888912038317), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00888912038317 UDI-DI	Date12 Aug 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00888912038317

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Procare
Generic name: Multifunction body cushion
Model / reference: 79-91100

Primary DI / UDI-DI: 00888912038317
FDA product code: LWG
GMDN term: Multifunction body cushion

Device class: Class I
Regulation number: 878.4950
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Multifunction body cushion.

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

Premarket exempt
Manufacturing date

Other properties (13, all answered No)