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Sleepsense 14837US-Kit

by S.L.P. Inc.

Sleepsense 14837US-Kit is a device made by S.L.P. Inc., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 07290012144844), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290012144844 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sleepsense
Generic name
Polysomnography analyser
Model / reference
14837US-Kit
Primary DI / UDI-DI
07290012144844
GMDN term
Polysomnography analyser
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polysomnography analyser

Other devices from S.L.P. Inc.

See all devices from S.L.P. Inc. →

Properties

  • Convenience kit
Other properties (14, all answered No)