Medical Dynamics, Inc.

Englewood, CO, US

Medical Dynamics, Inc. appears in FDA device records in Englewood, CO. FDA records list 18 510(k) clearances between 1988-10-13 and 1998-02-17, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 18
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 18 510(k) clearances for Medical Dynamics, Inc. between 1988 and 1998. The busiest year on record is 1989, with 5. The most recent is 1998, with 1.

Clearances by year, as a table

510(k) clearance decisions for Medical Dynamics, Inc., by decision year
Year	Clearances
1988	1
1989	5
1990	3
1991	2
1992	3
1993	1
1994	2
1998	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K974542	TRUE VISION, TRUE VISION II	EIA	Substantially Equivalent	1998-02-17
K921294	VIDEO ENDOSCOPE-RIGID MODIFICATION	HET	Substantially Equivalent	1994-07-20
K934682	SURGICAL VIDEO CAMERA AND ACCESSORIES	FWF	Substantially Equivalent	1994-02-15
K930568	ADAIR/VERESS NEEDLE INTRODUCER SET	GCB	Substantially Equivalent	1993-07-22
K915538	OVER THE WIRE STONE BASKET	LQR	Substantially Equivalent	1992-03-20
K914315	OPTICAL CATHETER INTRODUCER SETS, MODIFICATION	KGX	Substantially Equivalent	1992-03-04
K913986	CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM	FGE	Unknown	1992-01-28
K911296	OPTICAL CATHETER ARTHROSCOPE	HRX	Substantially Equivalent	1991-09-24
K903339	VIDEO ENDOSCOPE, RIGID	HET	Substantially Equivalent	1991-03-06
K904609	XENON LIGHT SOURCE	HBI	Substantially Equivalent	1990-12-18
K904113	OPERATIVE RECORDING CAMERA	IKO	Substantially Equivalent	1990-10-30
K900374	ADAIR/VERESS NEEDLE INTRODUCER SET	GCB	Substantially Equivalent	1990-04-20
K896008	MODEL 6500 MERCURY ARC LIGHT SOURCE	GCP	Substantially Equivalent	1989-12-27
K895041	OPTICAL CATHETER(TM) INTRODUCER SETS	KGZ	Substantially Equivalent	1989-10-16
K894319	MEDICAL DYNAMICS LIGHT SOURCE	FSW	Substantially Equivalent	1989-10-03
K891983	CAM-WRAP(TM) NEW STERILIZATION PROCEDURE	KCT	Substantially Equivalent	1989-04-19
K891236	FDX SOLID STATE VIDEO CAMERA MODEL 5950	FWD	Substantially Equivalent	1989-04-05
K884039	MEDICAL DYNAMICS SOLID STATE VIDEO CAMERA 5940	FWH	Substantially Equivalent	1988-10-13

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain