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Stablecut® 223502120

by Synvasive Technology, Inc.

Stablecut® 223502120 is a Class I device made by Synvasive Technology, Inc., listed in FDA GUDID since 24 Feb 2017 (UDI-DI 00846795023974), 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 Number00846795023974 UDI-DI Date24 Feb 2017ListedStatusListed 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  • Withdrawn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
Stablecut®
Generic name
Surgical saw blade, oscillating, single-use
Model / reference
223502120
Primary DI / UDI-DI
00846795023974
FDA product code
GFA
GMDN term
Surgical saw blade, oscillating, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Size
Width — 6 Millimeter
Length — 38 Millimeter

Related devices

Category: Surgical saw blade, oscillating, single-use

Similar devices in this category

Other devices filed under Surgical saw blade, oscillating, single-use.

Other devices from Synvasive Technology, Inc.

See all devices from Synvasive Technology, Inc. →

Properties

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