Home › Device types › FHG

Bell, Circumcision

FDA product code FHG · Class 2 · Obstetrics/Gynecology

34

Registered devices

42

Adverse events

0

Recalls

2

510(k) clearances

Devices with this code

PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.MABIS DMI — D-M-S HOLDINGS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.MABIS DMI — D-M-S HOLDINGS, INC.MABIS DMI — D-M-S HOLDINGS, INC.Centurion — CENTURION MEDICAL PRODUCTS CORPORATION MABIS DMI — D-M-S HOLDINGS, INC.MABIS DMI — D-M-S HOLDINGS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.Centurion — CENTURION MEDICAL PRODUCTS CORPORATION PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.Centurion — CENTURION MEDICAL PRODUCTS CORPORATION PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.MABIS DMI — D-M-S HOLDINGS, INC.MABIS DMI — D-M-S HOLDINGS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.Centurion — CENTURION MEDICAL PRODUCTS CORPORATION Centurion — CENTURION MEDICAL PRODUCTS CORPORATION PlastiBell Circumcision Device — ASPEN SURGICAL PRODUCTS, INC.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.