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LaserWrap A-100

by Spectra Therapy LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850083596026 UDI-DI Date24 Jul 2026ListedStatusListed 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  • Withdrawn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
LaserWrap
Generic Name
Musculoskeletal/physical therapy laser, professional
Model / Ref / Catalog
A-100
Primary DI / UDI-DI
00850083596026
FDA Product Code
ILY
GMDN Term
Musculoskeletal/physical therapy laser, professional
Device Class
Class II
Regulation Number
890.5500
GUDID distribution status
In Commercial Distribution

Other devices from Spectra Therapy LLC

Properties

  • Single Use
  • Prescription Use
  • Over-the-Counter
  • Premarket Exempt
  • Serial Number

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No