Skip to content

Stratafix Spiral SXMD2B150

by Surgical Specialties México, S. de R.L. de C.V.

Stratafix Spiral SXMD2B150 is a Class II device made by Surgical Specialties México, S. de R.L. de C.V., listed in FDA GUDID since 22 Oct 2015 (UDI-DI 10705031208148), 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 Number10705031208148 UDI-DI Date22 Oct 2015ListedStatusListed 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  • Withdrawn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
Stratafix Spiral
Generic name
Barbed polyester suture, non-antimicrobial
Model / reference
SXMD2B150
Primary DI / UDI-DI
10705031208148
FDA product code
GAM
GMDN term
Barbed polyester suture, non-antimicrobial
Device class
Class II
Regulation number
878.4493
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GAM (SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID).

Other devices from Surgical Specialties México, S. de R.L. de C.V.

See all devices from Surgical Specialties México, S. de R.L. de C.V. →

Properties

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