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Stealth Surgical SS1671821

by Boss Instruments, Ltd.

Stealth Surgical SS1671821 is a Class II device made by Boss Instruments, Ltd., listed in FDA GUDID since 1 Oct 2016 (UDI-DI 00888515263062), 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 Number00888515263062 UDI-DI Date1 Oct 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  • Withdrawn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
Stealth Surgical
Generic name
Surgical retractor/retraction system blade, reusable
Model / Ref / Catalog
SS1671821
Primary DI / UDI-DI
00888515263062
FDA product code
GZT
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class II
Regulation number
882.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical retractor/retraction system blade, reusable

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Other devices filed under Surgical retractor/retraction system blade, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)