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SourceMark SMCLIPPER

by Sourcemark, LLC.

SourceMark SMCLIPPER is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 18 Nov 2020 (UDI-DI 00813799007972), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813799007972 UDI-DI Date18 Nov 2020ListedStatusListed 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  • Withdrawn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
SourceMark
Generic name
Surgical hair clippers
Model / reference
SMCLIPPER
Primary DI / UDI-DI
00813799007972
FDA product code
LWK
GMDN term
Surgical hair clippers
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical hair clippers

Similar devices

Other devices filed under FDA product code LWK (Razor, Surgical).

Other devices from Sourcemark, LLC.

See all devices from Sourcemark, LLC. →

Properties

  • Supplied sterile
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)