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Surgistar 496106

by Surgistar Inc.

Surgistar 496106 is a Class I device made by Surgistar Inc., listed in FDA GUDID since 2 Aug 2016 (UDI-DI 00878799008060), 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 Number00878799008060 UDI-DI Date2 Aug 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  • Withdrawn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
Surgistar
Generic name
Eyelid speculum, reusable
Model / reference
496106
Primary DI / UDI-DI
00878799008060
FDA product code
HNC
GMDN term
Eyelid speculum, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eyelid speculum, reusable

Other devices from Surgistar Inc.

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  • Surgistar 8120

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See all devices from Surgistar Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)