Home › Device types › GAO
Suture, Nonabsorbable
FDA product code GAO · Class 2 · General, Plastic Surgery
378
Registered devices
601
Adverse events
1
Recalls
4
510(k) clearances
Devices with this code
Myo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONHu-Friedy Mfg. Co., LLC — HU-FRIEDY MFG. CO., LLCMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATIONMyo/Wire II — A & E MEDICAL CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-11 | EXP Pharmaceutical Services Corp | EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that |
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