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SharkCut T2650

by Techcord co., Ltd

SharkCut T2650 is a Class I device made by Techcord co., Ltd, listed in FDA GUDID since 15 Apr 2024 (UDI-DI 08800053401432), 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 Number08800053401432 UDI-DI Date15 Apr 2024ListedStatusListed 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  • Withdrawn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
SharkCut
Generic name
Arthroscopic shaver system blade, single-use
Model / Ref / Catalog
T2650
Primary DI / UDI-DI
08800053401432
FDA product code
GFA
GMDN term
Arthroscopic shaver system blade, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 5.0 Millimeter
Length — 128 Millimeter

Related devices

Category: Arthroscopic shaver system blade, single-use

Similar devices in this category

Other devices filed under Arthroscopic shaver system blade, single-use.

Other devices from Techcord co., Ltd

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)