Coherent Medical Group

Palo Alto, CA, US

Coherent Medical Group appears in FDA device records in Palo Alto, CA. FDA records list 27 510(k) clearances between 1985-01-03 and 1997-01-22, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 27
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 27 510(k) clearances for Coherent Medical Group between 1985 and 1997. The busiest year on record is 1985, with 5. The most recent is 1997, with 1.

Clearances by year, as a table

510(k) clearance decisions for Coherent Medical Group, by decision year
Year	Clearances
1985	5
1986	1
1987	5
1988	3
1989	2
1991	3
1992	2
1993	3
1994	1
1996	1
1997	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K963339	COHERENT ULTRAPULSE CO2 SURGICAL LASERS	GEX	Substantially Equivalent	1997-01-22
K960032	COHERENT VERSAPULSE AESTHETIC SURGICAL LASERS	GEX	Substantially Equivalent	1996-04-01
K932981	COHERENT VERSAPULSE 2.1 HOLMIUM SURGICAL LASERS	GEX	Substantially Equivalent	1994-05-02
K923575	COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS	GEX	Substantially Equivalent	1993-09-29
K932468	NOVUS MULTIWAVELENGTH	GEX	Substantially Equivalent	1993-09-22
K930981	ACCULITE(TM) OTOPROBE	GEX	Substantially Equivalent	1993-07-28
K914136	COHERENT VERSAPULSE(TM) 2.1XE/2.1L HOLMI SURG LASE	GEX	Substantially Equivalent	1992-07-21
K914991	VERSAPULSE(TM) TWOPOINTONE/XE HOLMIUM SURG LASERS	GEX	Substantially Equivalent	1992-05-06
K913127	COHERENT NOVUS 3000 ARGON PHOTOCOAGULATOR	GEX	Substantially Equivalent	1991-10-08
K910037	COHERENT HOLMIUM:YAG SURGICAL LASER	GEX	Substantially Equivalent	1991-09-25
K912029	ULTRAPULSE(TM) CARBON DIOXIDE SURGICAL LASER	GEX	Substantially Equivalent	1991-08-13
K893709	COHERENT MARIE ARGON PHOTOCOAGULATOR	HQF	Substantially Equivalent	1989-06-15
K885196	LASER INDIRECT OPHTHALMOSCOPE (LIO)	HQE	Substantially Equivalent	1989-01-11
K880603	COHERENT XA-40 CO2 SURGICAL LASER	GEX	Substantially Equivalent	1988-03-11
K874811	MODEL 5202 MICROMANIPULATOR	GEX	Substantially Equivalent	1988-02-05
K874648	COHERENT XA-30/SP CO2 SURGICAL LASER	GEX	Substantially Equivalent	1988-02-04
K873760	SUPERPULSE AMBULASE (XAM-SP) CO2 SURGICAL LASER	GEX	Substantially Equivalent for Some Indications	1987-11-27
K873246	MODEL 5001 MICROMANIPULATOR FOR USE W/TF-25 CO2	GEX	Substantially Equivalent	1987-11-10
K873963	COHERENT XA-30 CO2 SURGICAL LASER	GEX	Substantially Equivalent	1987-10-19
K870161	MODEL 5000 MICROMANIPULATOR MICRO CO2 LASER SYSTEM	GEX	Substantially Equivalent for Some Indications	1987-04-14
K870517	0.1MM, 0.25MM, 0.5MM, ZOOM DERMATOLOGIC HANDPIECE	GEX	Substantially Equivalent for Some Indications	1987-04-10
K862568	LDS - LASER DELIVERY SYSTEM	HQF	Substantially Equivalent	1986-10-07
K852860	MODEL 920 ARGON/DYE LASER-FOR DERMATOLOGICAL/USE	GEX	Substantially Equivalent	1985-10-07
K852190	MODEL 451 CO2 SURGICAL LASER	GEX	Substantially Equivalent	1985-08-23
K844357	SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR	HQF	Substantially Equivalent	1985-06-05
K844356	SYSTEM 930 ARGON PHOTOCOAGULATOR	HQB	Substantially Equivalent	1985-05-16
K844358	SYSTEM 920 PHOTOCOAGULATOR TO INCLUDE SCHIRMERSCOP	HQF	Substantially Equivalent	1985-01-03

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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What MDM checks, and what it does not

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