← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

LMG — Agent, Absorbable Hemostatic, Non-Collagen Based

DEVICE CLASS
Class III
REGULATION
21 CFR 878.4490
MEDICAL SPECIALTY
General, Plastic Surgery
REVIEW PANEL
SU
✓ Implant— Life-sustaining— GMP-exempt— Third-party review eligible
3
510(K)/PMA CLEARANCES
pma: 3
0
RECALL ENTRIES

Recent clearances

P050038Davol, Inc. · pma2026-07-15
N12159ETHICON, Inc. · pma2026-06-25
P210036Baxter Healthcare Corporation · pma2026-06-08

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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