Medical Device Manufacturer · US , Mchenry , IL

O.R. Specialties, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1981

Total

Cleared

Denied

O.R. Specialties, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1981 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by O.R. Specialties, Inc. Filter by specialty or product code using the sidebar.

O.R. Specialties, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - O.R. Specialties, Inc.

14 devices

1-12 of 14

Cleared Jul 06, 1994

LAPAROSCOPIC SCISSORS (DISPOSABLE)

K942607 · GEI

General & Plastic Surgery · 35d

Cleared Apr 06, 1994

PHACO NEEDLES 1000-R & 1000-O NEEDLES

K923630 · HQC

Ophthalmic · 624d

Cleared Aug 02, 1993

DISPOSABLE SCLERAL PLUGS

Ear, Nose, Throat · 199d

Cleared Oct 19, 1992

DISPOSABLE ENDOILLUMINATOR

K923774 · EQH

Ear, Nose, Throat · 83d

Cleared Aug 18, 1992

POLLY'S VITREOUS SCISSORS J-225-S

K922355 · HQE

Ophthalmic · 91d

Cleared Jul 02, 1992

LEWICKY O.R.S. TUBING

J105 JAMES SURGICAL SYSTEM I/A PACK

K911932 · GZX

Neurology · 118d

Cleared Aug 03, 1989

JAMES SURGICAL SYSTEM J1000

VITRECTOMY PACK #J120

K891161 · HQC

Ophthalmic · 81d

O.R. Specialties, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - O.R. Specialties, Inc.

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