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Tdm Surgitech, Inc.

FDA Regulatory Profile

Tdm Surgitech, Inc. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Tdm Surgitech, Inc." and its spelling variant "Tdm Surgitech".

Latest inspection: Nov 28, 2017 · VAI
Latest 510(k): May 28, 2015

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	1	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	1	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

Recent FDA inspections

1 inspection on Nov 28, 2017.

Date	Site	Product	Classification	FEI
Nov 28, 2017	Palm Harbor, FL	Devices	Voluntary Action Indicated (VAI)	3011680080

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3011680080	Palm Harbor, FL	1	Nov 28, 2017

Recent 510(k) clearances

1 510(k) clearance on May 28, 2015.

K-Number	Device	Date
K150824	TD-Wand	May 28, 2015

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