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VersaWrap Tendon Protector VTP2201

by Alafair Biosciences, Inc.

VersaWrap Tendon Protector VTP2201 is a Class II device made by Alafair Biosciences, Inc., listed in FDA GUDID since 23 Oct 2020 (UDI-DI B454VTP22011), 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 NumberB454VTP22011 UDI-DI Date23 Oct 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
VersaWrap Tendon Protector
Generic name
Tendon spacer
Model / Ref / Catalog
VTP2201
Primary DI / UDI-DI
B454VTP22011
FDA product code
OWW, FTM
GMDN term
Tendon spacer
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 2 Inch
Width — 2 Inch
Total Volume — 1 Milliliter

Related devices

Category: Tendon spacer

Similar devices

Other devices filed under FDA product code OWW (Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon).

Other devices from Alafair Biosciences, Inc.

See all devices from Alafair Biosciences, Inc. →

Properties

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