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Premium Plus 118

by Premium Plus International Limited

Premium Plus 118 is a Class II device made by Premium Plus International Limited, cleared under FDA 510(k) K163447 on 20 Jun 2017 and listed in FDA GUDID since 7 Jul 2017 (UDI-DI D8381182), active as of 22 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 22 Oct 2026

Documents

510(k) K163447

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD8381182 UDI-DI Date7 Jul 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK163447 Date20 Jun 2017DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K163447 decided 20 Jun 2017 Active
  • FDA GUDID UDI-DI D8381182 listed 7 Jul 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K163447
  2. Listed FDA GUDID D8381182

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Premium Plus
Generic name
Instrument/equipment drape, single-use, non-sterile
Model / reference
118
Primary DI / UDI-DI
D8381182
510(k) Number
FDA product code
PEM
GMDN term
Instrument/equipment drape, single-use, non-sterile
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code PEM (Dental Barriers And Sleeves).

Other devices from Premium Plus International Limited

See all devices from Premium Plus International Limited →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)