FDA applicant

Laser Media

Hauppauge, NY13 decisions1985–19870 recalls

FDA records 13 decisions for Laser Media (Hauppauge, NY) from 1985 to 1987: 12 510(k) clearances and 1 original PMA approval. Most are in product codes LNK (Laser For Gastro-Urology Use) and LLO (Laser, Neodymium:Yag, Pulmonary Surgery). No recall is linked to its devices.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Laser Media’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laser Media since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Laser”

FDA records each applicant name separately; these may or may not be the same firm.

Laser Industries, Ltd. 20 Laser Engineering, Inc. 18 L.A.S.E.R., Inc. 14 Laser Photonics, Inc. 14 Laser Peripherals, LLC 12 Laser-Optik-Systeme GmbH & Co. KG 7 Laser Spectrum, Inc. 5 Laser Max Medical Technologies Corp. 4 Laser Surgical Systems 3 Laser Associated Sciences, Inc. 2 Laser Dental Innovations 2 Laser Endo Technic 2

Laser Media

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Laser”