510(k) Report

FDA applicant

Britt Corp., Inc.

Los Angeles, CA17 decisions1979–20016 recalls

FDA records 17 decisions for Britt Corp., Inc. (Los Angeles, CA) from 1979 to 2001: 17 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and JOW (Sleeve, Limb, Compressible). 6 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Britt Corp., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Britt Corp., Inc. since 2007.

Recalls per year

6in 2019

2019: 6
2007high 6 (2019) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Britt Corp., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GEXPowered Laser Surgical Instrument3decisions
  • JOWSleeve, Limb, Compressible3decisions
  • EWGLaser, Ent Microsurgical Carbon-Dioxide2decisions
  • HQFLaser, Ophthalmic2decisions
  • LLFLaser, Neurosurgical, Argon1decision
  • DPSElectrocardiograph1decision

Also: HHR (1), IYO (1).

Who builds on its devices?

Later devices cite its devices 7 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K991038Vaso Press DVT System, Models VP500, VP501Britt Corp., Inc. · 20004cite it
  • K003828Vaso Press DVT Foot Garment #VP 520Britt Corp., Inc. · 20013cite it

What has FDA decided for it lately?

  • K003828Vaso Press DVT Foot Garment #VP 520Britt Corp., Inc. · 2001
  • K991038Vaso Press DVT System, Models VP500, VP501Britt Corp., Inc. · 2000
  • K974393Vaso Press SystemBritt Corp., Inc. · 19996 recalls
  • K860977Model 545-45 for Neurological Surgical ApplicationBritt Corp., Inc. · 1986
  • K860975Model 545-45 Laser for Ear, Nose & ThroatBritt Corp., Inc. · 1986
  • K860974Model 545-45 Laser for Derma., Pod., SurgicalBritt Corp., Inc. · 1986
  • K860277Model 525-25 Watt C02 Laser for Ear, Nose & ThroatBritt Corp., Inc. · 1986
  • K860273Model 525 - 25 Watt CO2 Medical Laser/PodiatryBritt Corp., Inc. · 1986

All 17 as Britt Corp., Inc. →

What has been recalled?

6 recalls linked to its devices; the latest:

  • K974393MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-SApr 8, 2019Class II
  • K974393MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, Model #6103S-SApr 8, 2019Class II
  • K974393MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model…Apr 8, 2019Class II
  • K974393MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-SApr 8, 2019Class II
  • K974393MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-SApr 8, 2019Class II
  • K974393MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model…Apr 8, 2019Class II