Avery Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avery Intl. - FDA 510(k) Cleared Devices
12
Total
6
Cleared
0
Denied
Avery Intl. has 6 FDA 510(k) cleared medical devices. Based in Painesville, US.
Historical record: 6 cleared submissions from 1986 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Avery Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avery Intl.
12 devices
Cleared
Feb 05, 1987
MEDICAL ADHESIVE TAPE AND ADHESIVE BANDAGE
General & Plastic Surgery
34d
Cleared
Feb 05, 1987
MEDICAL ADHESIVE TAPE & BANDAGE USING HYTREL FILM
General & Plastic Surgery
27d
Cleared
Feb 05, 1987
MEDICAL ADHESIVE TAPE & BANDAGE USING PCCE FILM
General & Plastic Surgery
27d
Cleared
Feb 04, 1987
IV SECUREMENT DEVICE
General & Plastic Surgery
33d
Cleared
Feb 04, 1987
IV SECUREMENT DEVICE USING HYTREL THERMO. FILM
General & Plastic Surgery
26d
Cleared
Feb 04, 1987
IV SECUREMENT DEVICE USING PCCE THERMO. FILM
General & Plastic Surgery
26d
Cleared
Feb 04, 1987
SURGICAL DRAPES AND ACCESSORIES USING HYTREL FILM
General Hospital
23d
Cleared
Feb 04, 1987
SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM
General Hospital
23d
Cleared
Feb 04, 1987
SURGICAL DRAPES AND ACCESSORIES USING PEBAX FILM
General Hospital
23d
Cleared
Jul 16, 1986
SURGICAL DRAPES AND DRAPE ACCESSORIES
General Hospital
20d
Cleared
Mar 03, 1986
ADHESIVE TAPE, WOUND CARE, WOUND DRESSING
General & Plastic Surgery
117d
Cleared
Mar 03, 1986
IV SECUREMENT DEVICES
General & Plastic Surgery
117d