FDA applicant

Super Glide, Inc.

Burlington, VT2 decisions1999–20010 recalls

FDA records 2 decisions for Super Glide, Inc. (Burlington, VT) from 1999 to 2001: 2 510(k) clearances. All are in product code KJJ (Cleanser, Root Canal). No recall is linked to its devices.

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

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

FDA decisions per year

No FDA decision for Super Glide, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Super”

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

Super Safe Plastic Products Co., Ltd. 6 Super Grow Lasers 2 Super Sagless Corp. 2 Super Optical, Inc. 1

Super Glide, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Super”