Medical Device Manufacturer · US , Sudbury , MA

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

8 submissions · 8 cleared · Since 1990

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.

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