Medical Device Manufacturer · US , Sudbury , MA

G.W.B. Intl., Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1990

Recent clearances: RITLENG BICAN.LACR.SETS/SELF THREAD. MONOKAS(CHG.IN STER.)

8

Total

8

Cleared

0

Denied

G.W.B. Intl., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Sudbury, US.

Historical record: 8 cleared submissions from 1990 to 1996. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by G.W.B. Intl., Ltd. Filter by specialty or product code using the sidebar.

G.W.B. Intl., Ltd. is one of 13208 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - G.W.B. Intl., Ltd.

8 devices

1-8 of 8

Cleared Mar 06, 1996

RITLENG BICAN.LACR.SETS/SELF THREAD. MONOKAS(CHG.IN STER.)

Ophthalmic · 93d

Cleared Oct 05, 1995

OPHTA SIL- PUNCTAL PLUGS (MODIFICATION)

Ophthalmic · 42d

Cleared Mar 14, 1995

OPHTA SIL {SELF-THREADING MONOKA (RITLENG TYPE)}

Ophthalmic · 41d

Cleared May 04, 1994

OPHTA SIL (RITLENG PROBE AND LACRIMAL INTUBATION SET)

Ophthalmic · 89d

Cleared Jun 18, 1991

OPHTA SIL(R), ENULCEATION/EVISCERATION IMPLANTS

Ophthalmic · 106d

Cleared May 13, 1991

OPHTA SIL (R), PUNCTAL PLUGS AND INSERTERS

Ophthalmic · 70d

Cleared May 01, 1991

OPHTA SIL (R), LACHRYMAL INTUBATION SETS

Ophthalmic · 58d

Cleared Jan 12, 1990

DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20

Radiology · 87d