§ COMPARE REGULATORS

MFDS vs HSA: Medical Device Regulatory Comparison

Compare the medical device registration pathways, classification, and regulatory requirements of MFDS (South Korea) vs HSA (Singapore).

MFDS

Ministry of Food and Drug Safety (South Korea)

South Korea

MFDS regulates medical devices in South Korea using a four-class system. The Korean Good Manufacturing Practice (KGMP) standard is required for all manufacturers. South Korea is an MDSAP participating

CLASSES

Class I, II, III, IV

PATHWAY

MFDS registration

KEY FUNCTIONS
  • KGMP compliance
  • Technical documentation review
  • MDSAP participation
  • Clinical trial approval
  • Device registration

HSA

Health Sciences Authority (Singapore)

Singapore

Singapore's HSA regulates medical devices using a four-class risk-based system (A, B, C, D). HSA accepts conformity assessment from recognized bodies and is a founding member of IMDRF. Singapore serve

CLASSES

Class A, B, C, D

PATHWAY

HSA registration

KEY FUNCTIONS
  • Device registration (Class B-D)
  • Class A dealer license
  • GN-13 guidance compliance
  • Adverse event reporting
  • IMDRF participation

MedFlux monitors both MFDS and HSA in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.

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§ OTHER COMPARISONS