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Greater Goods 0003

by Greater Goods, LLC

Greater Goods 0003 is a Class II device made by Greater Goods, LLC, cleared under FDA 510(k) K151206 on 28 Aug 2015 and listed in FDA GUDID since 18 Jan 2022 (UDI-DI 00875011000031), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K151206

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00875011000031 UDI-DI Date18 Jan 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK151206 Date28 Aug 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K151206 decided 28 Aug 2015 Active
  • FDA GUDID UDI-DI 00875011000031 listed 18 Jan 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K151206
  2. Listed FDA GUDID 00875011000031

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Greater Goods
Generic name
Pulse oximeter probe, reusable
Model / reference
0003
Primary DI / UDI-DI
00875011000031
510(k) Number
FDA product code
DQA
GMDN term
Pulse oximeter probe, reusable
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse oximeter probe, reusable

Similar devices in this category

Other devices filed under Pulse oximeter probe, reusable.

Other devices from Greater Goods, LLC

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Properties

  • Serial number
Other properties (14, all answered No)